11,15 dimethyl pge&#39; 1 &#39;and pgf&#39; 1&#39;

ABSTRACT

Prostaglandin E1-type and F1-type compounds of the formula   WHEREIN R is hydrogen or a hydrocarbyl group containing from 1 to 12 carbon atoms, inclusive, wherein W is   WHEREIN R7, R8, R9, R10, R11, R12, R13, and R14 are hydrogen or alkyl of 1 to 4 carbon atoms, inclusive, provided (1) that at least one of R7, R8, R9, R10, R11, R12, R13, and R14 is alkyl (2) that when R13 is alkyl, at least one of R7, R8, R9, R10, R11, R12, and R14 is alkyl, and (3) that when R7 is alkyl or when R7 and R8 are alkyl, at least one of R9, R10, R11, R12, R13, and R14 is alkyl; and the enantiomers and racemic mixtures thereof. These are useful for the same pharmacological purposes as the unsubstituted prostaglandins.

United States Patent 1 Pike et al.

[ 11,15 DIMETHYL PGE AND PGF [75] Inventors: John E. Pike; William P. Schneider,

both of Kalamazoo, Mich.

[73] Assignee: The Upjohn Company, Kalamazoo,

Mich.

[221 Filed: Dec. 8, 1972 [21] Appl. No.: 313,368

Related U.S. Application Data [60] Division of Ser. No. 123,370. March 11, 1971, abandoned which is a continuation-in-part of Ser. No. 648,992,.lune 26, 1967, abandoned.

{52] U.S. Cl. 260/514 D; 260/468 D [51] Int. Cl... C07c 61/32; C07c 61/36; C07c 69/74 [58] Field of Search 260/468 D, 514 D, 5 l4 UA [56] References Cited UNITED STATES PATENTS 3,296,091 l/l967 Beal et al. l95/3O Primary Examiner-Robert Gerstl 5 7 ABSTRACT Prostaglandin E -type and F -type compounds of the formula June 10, 1975 wherein R is hydrogen or a hydrocarbyl group containing from 1 to 12 carbon atoms, inclusive, wherein W is wherein R R R R R R R,;,, and R are hydrogen or alkyl of I to 4 carbon atoms, inclusive, provided (1) that at least one of R R R R R R R and R is alkyl (2) that when R is alkyl, at least one of R-,, R R R R R and R is alkyl. and (3) that when R is alkyl or when R, and R are alkyl, at least one of R R R R R and R is alkyl; and the enantiomers and racemic mixtures thereof. These are useful for the same pharmacological purposes as the unsubstituted prostaglandins.

9 Claims, No Drawings 1 11,15 DIMETHYL PGE, AND PGF CROSS REFERENCE TO RELATED APPLICATION This is a division. of application Serial No 123,370. filed March 11, 1971, now abandoned which was a continuation-in-part of our copending application Serial No. 648,992, filed June 16, 1967, and now abandoned.

BRIEF SUMMARY OF INVENTION This invention relates to racemic and optically active prostaglandin analogs of the formula wherein R is hydrogen or a hydrocarbyl group containing from 1 to 12 carbon atoms, inclusive, wherein wherein R R R R R R R and R are hydrogen or alkyl of l to 4 carbon atoms, inclusive, provided l that at least one of R R R R R R R and R is alkyl (2] that when B, is alkyl, at least one of R R R R R R and R is alkyl, and (3) that when R, is alkyl or when R, and R are alkyl, at least one of R R R R R and R is alkyl; and the enantiomers and racemic mixtures thereof; from unsaturated fatty acids of the formula wherein R is H or hydrocarbyl, R,, R R R R and R,,- are H or CH;; m is an integer from 1 to 7, inclusive, n is or 1. and p is an integer from I to 7, inclusive; and processes for preparing them, for example by oxidation with singlet oxygen to form peroxide intermediates followed by reduction or disproportionation of the peroxide intermediate or by biological oxidation.

The compounds of this invention and processes for their production can be represented by the following sequence of formulas:

"on" s i I i i nac OH cccH-c C-CmH.m-CH= HO wherein R, R R R R R R m, n and p are as given above.

In the process of this invention all the compounds having one or more assymmetric carbon atoms can be produced as racemic mixtures. Those racemic mixtures which are obtained can be resolved at appropriate stages by methods well known in the art.

It is to be understood that the pictorial representation of the compounds in the flow sheet above is to be construed as inclusive of other forms including enantiomers and racemates, and not to be construed as limited to the particular form shown. The starting materials for the process of this invention are unsaturated fatty acids of formula I. Many acids of this formula occur naturally, for example linolenic, bis-homo-y-linolenic, and arachidonic acids. The natural acids, and the acids of formula I which do not occur in nature, can be prepared by synthetic methods. for example as shown by Osbond. Progress in the Chemistry of Fats and Other Lipids, Vol. 9, p. l2 l, l966, and in the preparations below.

The process of this invention comprises the follow- The compounds of formula 1, for example bis-homo y-linolenic acid, are treated with singlet oxygen to produce a mixture of the compounds of formula 2 and 3, for example racemic 7-l3a, 5a-peroxy-2B-(2-octenyl)- cyclopent-layl]heptanoic acid (2) and racemic 7- [3a,50zperoxy-2B-(3-hydroperoxyl-octeny)-cyclopent-la-yflheptanoic acid (3). The relative proportions of compounds 2 and 3 will vary depending upon the substrate, the reaction conditions, and the amount of oxidant. A small excess of oxidant and mild reaction conditions will favor the production of compounds of formula 2 and a larger excess of oxidant and more severe conditions will result in the formation of mostly compounds of formula 3. The oxygenated products of structures 2 and 3 can be isolated by methods known to be useful in the isolation of products obtained by photochemical oxidations. In many instances it is preferred not to isolate these intermediate peroxy compounds but to transform the product in situ to the subsequent oxygenated products of this invention. Compounds 2 and 3 can be separated by means known in the art, for example by chromatography over acid washed silica gel, chromatography over silver-nitrate impregnated silica gel, preparative thin layer chromatography, and the like. The compounds of formula 2 can be transformed to the compounds of formula 3 by repeating the oxidation with singlet oxygen.

The use of singlet oxygen as a selective chemical reagent is known in the art. A number of methods are available for generating singlet oxygen, for example: I Photo-oxygenation in the presence of a photosensitizer such as chlorophyll, hematoporphyin, Rose Bengal, eosin and the like, as described by A. Nickon and W. L. Mendelson, J. Am. Chem. Soc. 87, 392l (1965) and K. Gollnick and G. O. Schenk, Pure and Applied Chem., 9,507( 1964), or as described in US. Pat. No. 3,281,4l5. 2) Electrodeless discharge of gaseous oxygen, as described by E. J. Corey and W. C. Taylor, J. Am. Chem. Soc. 86, 3881 (l964). 3) Use of hypochlorites and hydrogen peroxide. This method is described by C. S. Foote and S. Wexler, J. Am. Chem. Soc. 86, 3879 and 388l (1964), and in US. Pat. No. 3,274,181. 4) Use of the benzyl cyanide; hydrogen peroxide; base system, described by E. McKeown and W. A. Waters, Nature, 203, 1063 (i964). 5) Use of hydrogen peroxide and oxalyl chloride, as described by E. A. Chandross, Tetrahedron Letters, 12, 761 (1963), and Corey, cited above. 6) Use of ozone and phosphines, phosphites, etc, as given by Q. E. Thompson, J. Am. Chem. Soc. 83, 845 H961) and Corey, cited above. 7) By the reaction of hydrogen peroxide in aqueous solution with Fe T (III), or Ce (IV) ions, described by Stauff and Lohman, Z. physikal Chem., N. F.. 40, 123 (1964) and 8) By pyrolysis of aromatic endoperoxides, such as anthracene or tryptycene endoperoxide. The 9,10- diarylanthracene endoperoxides are especially useful.

In all the reaction mixtures described above, addition of autoxidation inhibitors results in improved results in the process of this invention, by decreasing autoxidation side reactions with ordinary oxygen. Suitable antioxidants are phenol, hydroquinone, vitamin E, 2,6-di-t buty-phenol and, preferably, 2,6-di-t-butyl-4- methylphenol.

In some cases it is advantageous to add a metal salt as a catalyst for the singlet oxygen oxidation. Suitable metal ions are Cu, Cu, Co, Fe, Pd, Pt, gfl CZ++, Ce and Ti? These salts can, for example, be chlorides. bromides, sulfates, nitrates, and the like.

The compounds of formula 3, for example racemic 7-[3a, 5a-peroxy-2B-(3-hydroperoxy-l-octenyl)cyclopentl a-yllheptanoic acid, are transformed to the compounds of formula 4, for example, racemic 7-[3a,5adihydroxy-2B-( 3-hydroxyl -octenyl )cyclopentl ayl]heptanoic acid (racemic PGFla), by mild reduction. Suitable reducing agents are metal hydrides, for example sodium and potassium borohydrides, thiourea, sodium sulfite, zinc dust and acetic acid, hydrogen in the presence of a catalyst, triphenylphosphine, and the like. An excess of reducing agent is ordinarily employed, and appropriate solvents and temperatures are employed as well known in the art for the use of these reducing agents.

Very mild reduction of compounds of formula 3 results in the reduction of the hydroperoxy group on the side chain without destroying the peroxy ring compound, giving compounds designated 3a, for example racemic 7[ 3a,5a-peroxy-2B-( 3-hydroxyl octenyl)cyclopent-la-yHheptanoic acid (3a) is obtained from racemic 7-[ 3a,50z-peroxy-2B-( 3- hydroperoxyl -octenyl )cyclopentl oz-yl]heptanoic acid (3). This selective reduction can be obtained using about one equivalent, or a small excess over one equivalent, of the reducing agents named for the reduction of compound 3 to compound 4, or by the use of an alkali metal iodide and sodium thiosulfate as a reducing agent. The resulting peroxy compounds can be isolated as described above for compounds of formulas 2 and 3, or can be carried through the next step in situ. The compounds designated 3a (wherein R is hydrogen) on treatment with a slightly basic chromatographic alumina, or a mild base such as pyridine, potassium acetate in ethanol and the like, are converted to compounds of formula 5, for example racemic 7-[301- hydroxy-5-oxo-2B-( 3 hydroxy' l -octenyl )cyclopentla-yl]heptanoic acid (5) (racemic PGE, The conversion of the compounds designated 3 to the compounds of formula 5 can also be carried out by the action of heat, by irradiation with ultraviolet light, and by the action of titanous chloride in the presence of an acidic catalyst as shown by Paget. J. Chem. Soc. 829 (I938) and Davis et. al., Proc. Chem. Soc. 83 (l96l Alternatively the compounds of formulas 4 and 5 can be prepared from the compounds of formula 2 by first reducing or isomerizing the peroxide ring, and then introducing the side chain hydroxyl group. Treating compounds of formula 2, for example racemic 7- l 3a,5a-peroxy-2B(2octenyl)cyclopent-1a-yl]- heptanoic acid, with a reducing agent as described above for the conversion of compounds of formula 3 to the compounds of formula 4 produces compounds of formula 8, for example racemic 7-[3a,5a-dihydroxy- 2B-( 2-octenyl )cyclopent-la-yl Iheptanoic acid] (8). Treating compounds of formula 8 with singlet oxygen as described above for the conversion of compounds of formula 2 to the compounds of formula 3, produces compounds of formula 9, for example racemic 7- [3a,5 a,di-hydroxy-2B-( 3-hydroperoxyl octenyl)cyclopent octenyl)cyclopent yl] heptanoic acid, which are then treated with a reducing agent, in the manner described above for the production of compounds of formula 4 from compounds of formula 3, to produce compounds of formula 4, for example racemic 7-[ 3a,5a-dihydroxy-2B-( 3-hydroxyl -octenyl cyclopent-la-yl]-heptanoic acid (4). Treating compounds of formula 2 wherein R is hydrogen with a base or another isomerizing agent as described above for the production of the compounds of formula 5 from the compounds designated 3a produces the compounds of formula 6, for example racemic 7-[3a-hydroxy-5-oxo- 2/3-(2-octenyl)cyclopent-la-yllheptanoic acid (6). Treating compounds of formula 6 with singlet oxygen as described above for the conversion of compounds of formula 2 to the compounds of formula 3 produces compounds of formula 7, for example racemic 7-[3ahydroxy-5-oxo-2B-(3-hydroperoxy-1-cotenyl)cyclopent-la-yl1heptanoic acid (7), which are then treated in the manner described above for the production of compounds of formula 4 from the compounds of formula 3 with a reducing agent to produce compounds of formula 5, for example racemic 7-[3a-hydroxy-5-oxo- 2B-( 3-hyd roxl -octenyl )cyclopentl a-yllheptanoic acid (5).

All of the compounds of this invention can be isolated and purified by conventional methods. Isolation can be accomplished, for example, by dilution of the reaction mixture with water, extraction with a waterimmiscible solvent, such as methylene chloride, ethyl acetate, benzene, cyclohexane, ether, toluene and the like, chromatography, adsorption on ion-exchange resins, distillation, or a combination of these. Purification of the compounds of this invention can be accomplished by means known in the art for the purification of prostaglandins and lipids, fatty acids, and fatty esters, for example reverse phase partition chromatography, countercurrent distribution, adsorption chromatography on acid washed Florisil (synthetic magnesium silicate) and acid washed silica gel, preparative paper chromatography, preparative thin layer chromatography, chromatography over silver loaded cation exchange resins, and combinations thereof can be used effectively to purify the compounds produced by the processes of this invention.

The starting unsaturated fatty acids may, if desired, be esterified and the esters can be carried through the steps of the invention as shown in the flowsheet above, except in those singlet oxygen processes involving alkaline reaction conditions. The compounds of formulas 4, 5, 6 and 8 can also be esterified. The esterification is preferably carried out by reacting the selected acid with a diazoalkane, e.g. diazomethane, diazoethane, diazobutane, l-diazo-2-ethylhexane, cyclohexyldiazomethane, diazododecane, and the like, in the presence of an inert organic solvent such as methanol, diethyl ether, tetrahydrofuran and the like at about 0 to C.

The racemic products and intermediates of this invention can be resolved into their optically active components by a number of methods of resolution well known in the art. For example, the free acids can be treated with an optically active base such as cinchonine. quinine. brucine. dor l-(x-phenylethylamine and the like to produce diastcreoisomeric salts which can be separated by crystallization. Alternatively the acid may be esterified with an optically active alcohol and the products resolved. Resolution can also be accomplished by selective transformation of one isomer with a biologically active prostaglandin transforming systern. for example. the IS-dehydrogenating system present in lung such as guinea pig. rat and pig lung and in microorganisims such as fungi. Such transformations can be carried out by incubation or perfusion using methods well established in the art. followed by isolation and recovery of both the isomer resistant to the metabolic transformation applied and the product formed by the enzymatic transformation.

Til nrocess of this invention produces racemic prostaglanozn. corresponding otherwise to natural prostaglandins when bis-homo-y-linolenic acid or arachi donic acid are used as the starting material. and derivatives or analogs of the natural prostaglandins when other unsaturated acids of formula 1 are used as starting materials.

The prostaglandins are a family of closely related compounds which have been obtained from various animal tissues. and which stimulate smooth muscle. lower arterial blood pressure, antagonize epinephrineinduced mobilization of free fatty acids. and have other pharmacological and autopharmacological effects in mammals. including man. Se Bergstrom et al.. J. Biol. Chem. 238. 3555 (1963). Horton. Experientia, 21. l l3 l965 and references cited in those for discussions of the occurrence. structure, and properties of the prostaglandins.

All of the so-called natural prostaglandins are derivatives of prostanoic acid:

-istry at C-8 and C-l Z is indicated in accord with Nugteren et al.. Nature. 212. 38 (1966).

One significant characteristic of these natural prostanoic acid derivatives is the length of the multi-carbon side chains attached to C-8 and to C4 2. In prostanoic acid and in each of the prostaglandins obtained from animal tissues. the chain attached to C-8 always contains seven carbon atoms and the chain attached to C12 always contains eight carbon atoms.

The compounds of formulas 4 and 5 in which the length of the side chains corresponds to the side chains of prostanoic acid exhibit hypotensive and smooth muscle stimulating activity. The hypotensive activity of these compounds makes them useful in the control of hypertension in birds and mammals. including humans and valuable domestic animals. and in laboratory animals such as rats. mice, and rabbits. They also possess activity as fertility controlling agents. central nervous system regulatory agents. saltand water-retention regulatory agents, fat metabolic regulatory agents and as serum cholesterol lowering agents which latter activity makes these compounds useful in prevention of the onset of atherosclerosis and also in the treatment thereof in birds and mammals, including humans and valuable domestic animals. The activity of said compounds as fat regulatory agents makes them useful in the control of obesity.

The compounds of formulas 4 and 5 which are analogs or derivatives of the natural prostaglandins have prostaglandin-like activity which includes but is not limited to smooth muscle stimulation, vasodepressor activity. and inhibition of triglyceride breakdown in adipose tissues.

In comparison with the natural prostaglandins. the analogs and derivatives of this invention are substantially more specific in causing prostaglandin-like biological responses. and their use for desired pharmacological purposes results in substantially smaller and/or fewer undesired side effects. Therefore, the prostaglandin analogs and derivatives of this invention are useful as pharmacological agents for the control of hyperten sion. to block mobilization of free fatty acids, and to stimulate smooth muscle in mammals. including man, valuable domestic animals. and laboratory animals.

Compounds of formulas 4 and 5. wherein one or more of the groups R R R;,. R R and R is an alkyl radical of l to 4 carbon atoms, inclusive. rather than hydrogen. or wherein l or 2 alkyl radicals of l to 4 car bon atoms. inclusive are present in C,,.H2,,, adjacent to the side chain C-OH. especially compounds so substituted and wherein the lengths of the two main side chains are the same as for prostanoic acid, have unexpectedly decreased rates of metabolic destruction and consequently longer durations of the desired activity. In addition these particular compounds are substantially and unexpectedly more specific in causing de sired prostaglandindike biological responses and their use for pharmacological purposes results in substantially smaller and/or fewer undesired side effects.

The compounds of formulas 4 and 5 can be administered orally, parenterally. or intravenously. For example. a compound can be administered by intravenous infusion of a sterile isotonic saline solution at the rate of about 0.0l to about 10. preferably about 0.05 to about 5, micrograms per kilogram of animal body weight per minute.

The products and intermediates of this invention when produced by singlet oxygen oxidation of unsaturated fatty acids, as described above. are racemic mixtures. Optically active products and intermediates can be obtained by resolution of these mixtures. as described above. In addition. the optically active products 4 and 5. with the configuration shown in the flowsheet above. are produced by biological oxidation of the starting materials of formula l following the procedures given in US. Pat. No. 3.290.226 or US. Pat. No. 3.296.09l. For example. the novel branched chain prostaglandins 7-! -loz-hydroxy-5-oxo-2B-( 4methyl3-hydroxyl octcnyl)-cyclo-pe.it layl lheptanoic acid,

7-l 3a.5rx-dihydroxyQ84 4 methyl3 hydroxyl octenyl )cyclopentlor-yl Iheptanoic acid.

7-[ 3a-hydroxy-5-oxo-2B-(4,4-dimethyl-3 hydroxy- 1 octenyl )-cyclopentl oz-yllheptanoic acid, 7-[ 3a,5a-dihydroxy-2B-(4.4-dimethyl-3-hydroxy-1- octenyl )-cyclopent- I a-yllheptanoic acid. 7-[3a-hydroxy-5-oxo-2B-(3-hydroxy-3-methyl-loctenyl )-cyclo-pentlat-61 ]heptanoic acid. 7-[ 3a.,5a-dihydroxy-2B-( 3-hydroxy-3-methyll octenyl )cyclopentl oz-yl heptanoic acid, 7-[3a-hydroxy-3B-methyl-5-oxo-2B-(3-hydroxy-3- methyl-1-octenyl)-cyclopent-la-yl]heptanoic acid. 7-[ 3a,5a-dihydroxy-3B-methyl-2B-( 3-hydroxy-3- methyl- 1 -octenyl)-cyclopent-l a-yl1heptanoic acid, 7-[ 3a-hydroxy l [3,2A-dimethyl--oxo-2/3-( 3-hydroxy- I-octenyI)-cyclopent-la-yl]heptanoic acid and 7-[ 3a,5a-dihydroxy-l,8,2B-dimethyl-2,B-(3-hydroxy-1- octenyl )-cyclopent-la-yl]heptanoic acid are obtained by substituting the corresponding branched chain unsaturated fatty acids, l6-methyl-8,l l,l4-eicosatrienoic acid, l6,l6-dimethyl-8,l l,l4-eicosatrienoic acid, l5-methyl-8.l 1.1 4-eicosatrienoic acid. I l,15-dimethyl-8,l l,l4-eicosatrienoic acid. and 3.l2-dimethyl 8,l l,l4-eicosatrienoic acid for arachidonic acid In Example I of US. Pat. No. 3,290,226 or Example I of US. Pat. No. 3.296.091.

DETAILED DESCRIPTION In the examples which follow, the progress of the reaction and the purification procedures can advantageously be followed by thin layer chromatographic analysis. Apreferred procedure is to use silica gel plates developed with ethyl acetate and sprayed with sulfuric acid to detect the spots.

In some of the preparations which follow. nuclear magnetic resonance spectroscopy (N.M.R.) has been used to characterize and define the products obtained. All N.M.R. data were obtained on the Varian N.M.R. instrument. Model A-60 (run at 60 megacycles) and reported in cycles per second (cps) downfield from the standard tetramethylsilane.

Preparation l Cis.cis. cis-9,l2,l5-heneicosatrienoic acid.

A. lBromo-o-chlorohexane Following the procedure of Cloke, et al.. J. Am. Chem. Soc. 53, 2794 (1931), hexamethylene chlorohydrin was converted to Lbromo-6-chlorohexane, b.p. 6668C./lmm., N =l.4795.

Anal. Calcd. for C H BrCI: C. 36.l I; H, 6.06.

Found; C. 37.ll; H, 6.05.

B. 8-Chloro-l-octyne To about 450 ml. of liquid ammonia saturated with acetylene was added slowly 15.5 g. of sodium with continued addition of acetylene so that the solution remained colorless. After all the sodium had dissolved addition of acetylene was ended and the acetylene delivery tube was removed. then a dry-ice acetone condensor was fitted and 135 g. of l-bromo-6- chlorohexane was added dropwise. The ammonia refluxed vigorously during the addition of the l-bromo-6- chlorohexane. After the addition was completed the mixture was stirred for two hours, then 200 ml. water was added slowly and the mixture was allowed to warm to room temperature and extracted with ether. The ether extract was washed with water. 3N hydrochloric acid, and aqueous sodium bicarbonate, then was dried over sodium sulfate and evaporated to leave a residue which was distilled under reduced pressure. The major fraction collected, 84 g., comprised 8-chloro-l-octyne boiling at 60-65C./l0mm. and showing infrared absorption maxima at 3270, 212.0 and 735 cm.

Anal. Calcd. for C H Cl: C. 66.43; H. 9.06; C],

24.52. Found: C. 65.53; H, 8.60; CI. 25.07. C. l-Chloro-7. I0, I 3-nonadecatriyne To 13.3 ml. of 3M ethyl magnesium bromide in 30 ml. of dry tetrahydrofuran was added a solution of 5.8 g. of 8-chloro-l-octyne in 10 ml. of dry tetrahydrofuran. The mixture was refluxed under nitrogen for 30 min., then stirred at room temperature (about 25C.) for 30 min., and 0.25 g. of powdered dry cupious chloride was added. The mixture was stirred for 20 minutes, then a solution of 8.98 g. of l-br0mo-2.5-undecadiyne in 10 ml. of dry tetrahydrofuran was added, and the reaction mixture was stirred and heated under reflux for 10 hrs. during which a yellow precipitate formed. The entire mixture was poured into saturated aqueous ammonium chloride and ether, filtered through Celite (diatomaceous earth filter aid), and the ether solution was separated, washed with water. dried over sodium sulfate, and evaporated to give a residue comprising 1- chloro-7,l0,l3-non-adecatriyne. The thus obtained residue was distilled in a short path distillation flask up to l50/0.005 mm. to remove starting materials, then was distilled in a short path tube, bath temperature up to 190/0.004 mm. to give l-chloro-7,l0.l3- nonadecatrivne as a yellow oil, which crystallized when stored at -l0C., and had the following analysis:

I.R. (principal bands): l3l5. 1220 and 730 cm'l. N-M-R.: 212 cps. (triplet l=7 cps.), l87.5 cps. (quintet r .l=2.5 cps). I30 cps. (multiplet) 54 cps. (triplet J=6 cps). d. l-Chloro-cis.cis.cis-7,l0,13-nonadecatriene A mixture of 35.9 g. of l-chloro-7.l0,l 3- nonadecatriyne dissolved in 200 ml. of pyridine and 5.4 g. of 5 percent palladium on barium sulfate was shaken in an atmosphere of hydrogen in a Parr hydrogenator for 1.25 hrs. (pressure drop 2l.5 lb.; 0.1 mole hyrogen 8.5 lb.). then the reaction mixture was poured into water and extracted with ether. The ether extract was washed several times with water, then with dilute hydrochloric acid, followed by saturated aqueous sodium chloride. The ether solution was then dried over sodium sulfate, and evaporated under reduced pressure leaving a residue comprising l-chloro-cis.cis,cis 7,l0.l3-nonadecatriene which was further purified by distil lation on a shaking short path distillation apparatus, giving 27 g. of l-chloro-cis.cis,cis-7,l0.l3- nonadecatriene collected at a jacket temperature of l-l90/0.005 mm.

Anal. Calcd. for C H Cl: C. 76.85; H, 11.20; Cl,

11.94. Found: C, 76.38; H. 12.98; Cl, ll.88. E. Cis,cis,cis-9.12.15-heneicosatrienoic acid To 15 ml. of n-butanol under nitrogen was added 2] l mg. of sodium in pieces. The mixture was heated gently until all the sodium had dissolved, then l.2 ml. of diethylmalonate was added and the mixture was refluxed one hour. then cooled, and a solution of 2.0 g. of lchloro-cis,cis,cis-7,l0.l3-nonadecatriene in 7.5 ml. of n-butanol was added. The resulting reaction mixture was refluxed for 3 hrs. under nitrogen, then allowed to stand for about 20 hrs., and concentrated under reduced pressure. The thus obtained residue was dissolved in a solution of 1.9 g. of potassium hydroxide in 38 ml. of 95 percent ethanol and heated under reflux for 3.5 hrs., then was concentrated to about l/3 volume, diluted with water, and extracted with ether. The ether solution was extracted with 1N aqueous sodium hydroxide. The sodium hydroxide solution was made acid with 3N hydrochloric acid and extracted twice with ether. The ether extracts were washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated to give 1.72 g. of a pale yellow oil. The thus obtained oil was heated in a short path distillation tube at 140C. under reduced pressure until decarboxylation was complete, then was distilled at a bath temperature of l80-200/0.006 mm., thus obtaining a distillate comprising cis,cis,cis- 9,12,15-heneicosatrienoic acid. Preparation 2. 15 methyl-8,1l,l4 elcosatrienoic acid A. 3-Hydroxy-3-methyl-l-octyne A solution of 46.5 g. of Z-heptanone in 56 ml. of tetrahydrofuran was added slowly, with stirring, to a mixture of 45.5 g. of lithium acetylide ethylene diamaine, 200 ml. of dry tetrahydrofuran and 200 m1. of benzene at 35C. under nitrogen. Stirring was continued for 2.5 hrs. after addition of the Z-heptanone was completed, then 130 ,ml. of water was added slowly and the mixture was heated under reflux for 1 hour. The mixture was cooled and extracted with ether. The ether extract was washed with water, 1N hydrochloric acid, aqueous sodium bicarbonate, saturated aqueous sodium chloride, dried over Na SO,, and evaporated. The thus obtained residue was distilled through a Vigreaux column, giving 36 g. of 3-hydroxy-3-methyl-l-octyne having a boiling point of 8590C. at 28 inches of mercury.

B. 3-Hydroxy-3-methyll-octene A mixture of 20 g. of 2-hydroxy-2-methyl-l-octyne, 500 mg. of 5 percent palladium on barium sulfate catalyst, and 200 ml. of pyridine was shaken under hydrogen, at an initial pressure of 45 lb./sq. in. at room temperature (about 25C.). The hydrogenation was stopped after 20 min., at which time the pressure drop corresponded to the calculated amount for 1 mole of hydrogen uptake per mole of compound. The reaction mixture was poured into water and extracted with ether. The ether extract was washed with water, dilute hydrochloric acid, aqueous bicarbonate, dried over sodium sulfate, and evaporated. The thus obtained residue was distilled through a Vigreaux column and 15.5 g. of distillate comprising 3-hydroxy-3-methyl-1-octene having a boiling point of 8990C. at 28 inches of mercury was collected.

Anal. Calcd. for C H O: C, 75.99; H, 12.76.

Found: C, 75.56; H, 12.82.

C. 1-Bromo-3-methy1-2octene In an ice-salt bath 25 ml. of 48 percent hydrobromic acid was saturated with hydrogen bromide by bubbling through for 5-10 minutes, then g. of 3-hydroxy-3- methyH-octene was added slowly with stirring. The mixture was stirred an additional min. then benzene was added and the benzene layer was separated, washed with ice water, aqueous sodium bicarbonate, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated to give a residue. The thus obtained residue was distilled through a Vigreaux column, collecting a main fraction weighing 11 g. comprising 1 bromo-3-methyl-2-octene boiling at 95-l 10C. at 28 inches of mercury.

12 Anal. Calc'd for C H Br'. C, 52.69; H, 8.35; Br,

Found: C, 52.58; H, 8.40; Br, 38.59.

D. 6-Methylundec-2-yn-5-en-l-ol A solution of 5.6 g. of propargyl tetrahydropyranyl ether in 40 ml. of dry tetrahydrofuran was added slowly, with stirring to 14 ml. of 3 M ethyl magnesium bromide in ether under nitrogen. The mixture was heated under reflux for 1 hr., then was cooled and 120 mg. of powdered cuprous chloride was added. After stirring for 20 mins., a solution of 8.0 g. of 1-bromo-3- methyl-2-octene in 8 ml. of tetrahydrofuran was added. The mixture was heated under reflux for 2 hrs., then cooled, and 20 ml of saturated aqueous ammonium chloride was added slowly. Ether was added, and the mixture was filtered through Celite (diatomaceous earth filter aid), then the ether layer was separated, washed with water, dried over sodium sulfate, and evaporated giving a residue. The thus obtained residue was heated under reflux for two hours in 24 ml. of methanol containing 148 mg. of p-toluene-sulfonic acid, then the mixture was cooled, diluted with water, and extracted with ether. The ether extract was washed with aqueous sodium bicarbonate, aqueous saturated sodium chloride, dried over sodium sulfate, and evaporated leaving a residue. The residue was distilled and gave 4.0 g. of a mixture comprising 6-methylundec-2-yn-5-en-1-o1, b.p. 9610lC./ 0.006

E. 1-Bromo-6-methylundec-Z-yn-S-ene A mixture of 17 g. of 6-methylundec-2-yn-5-en-l-ol, 32.4 ml. of ether, and 2.07 ml. of pyridine was stirred under nitrogen in an ice-salt bath and 4.5 m1. of phosphorus tribromide was added. The ice-salt bath was then removed and the mixture was first allowed to warm to room temperature, then was heated under reflux for 2.5 hrs. The mixture was again cooled in an ice bath, and 15 ml. each of ether and water were added. The ether layer was separated, washed with aqueous sodium bicarbonate, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated. The thus obtained residue was distilled, collecting 14 g. of a mixture comprising l-bromo-6-methylundec-2-yn- S-ene at 85-89C./0.005 mm.

F. 1-Ch1oro-l4-methyl-nonadeca-7,l0-diyn-l 3-ene To 21 ml. of 3M ethereal methyl magnesium bromide in 47.5 ml. of dry tetrahydrofuran under nitrogen was added 9.2 g. of 1-ch1oro-7-octyne in 15 m1. of tetrahydrofuran. The mixture was heated under reflux for 30 min., then was allowed to cool to room temperature during another 30 minutes after which 365 mg. of cuprous chloride was added. The mixture was heated under reflux for 20 min., then a solution of 14 g. of 1- bromo-b-methyl-undec-2-yn Sene in 12.9 ml. of tetrahydrofuran was added. The mixture was heated under reflux for 10 hrs., then cooled in an ice bath and 250 ml. saturated aqueous ammonium chloride was added. Ether was added and the mixture was filtered through Celite (diatomaceous earth filter aid) and separated. The thus obtained ether layer was washed with saturated aqueous sodium chloride, dried with magnesium sulfate, and evaporated. The thus obtained residue was distilled through a rocking short-path distillation apparatus, collecting 11.5 g. of a mixture comprising 1- chloro-14-methy1nonadeca-7,IO-diyn-l 3-ene at a bath temperature of l-l90/0.()05 mm.

Anal. Calcd. for C ll-M C]: C], 11.55.

Found: Cl, 12.59

F. 1-Chloro-l4-methyl-7,10,13-nonadecatriene A mixture of 1 1.0 g. of 1-chloro-14-methylnonadeca-7,l-diyn-l3 ene, 1.5 g. of percent palladium on barium sulfate, and 80 ml. of pyridine was shaken in a Parr rocker under 40 lb. of hydrogen pressure for about 1.3 hrs. at which time two moles of hydrogen had been absorbed. The reaction mixture was then poured into water and extracted with ether. The extract was washed with water, dilute hydrochloric acid, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated leaving a residue comprising l-chlorol 4-methyl-7, l 0, l 3-nonadecatriene. The residue was distilled in a rocking short-path distillation apparatus, collecting 7.6 g. ofa mixture comprising l-chloro-l4-methyl-7,l0,l3-nonadecatriene at a bath temperature of 180C. and a pressure of 0.005

C]. Methyl l5-methyl-8,l1,14-eicosatrienoate A mixture of 7.5 g. of l-chloro-14-methyl-7,l0,l3- nonadecatriene, 7.5 g. of potassium cyanide, and 36.8 ml. of dimethyl-sulfoxide was stirred and heated under nitrogen for 2.5 hrs. at 115C. The mixture was then poured into water and extracted with ether. The ether extract was washed with water, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated leaving a residue. The thus obtained residue was cooled in an ice bath and mixed with 54 ml. of 25 percent hydrogen chloride in methanol containing 0.6 ml. of water. The ice was allowed to melt and the mixture was stirred 'for about 18 hrs., then was poured into water and extracted with ether. The ether extract was washed with water, aqueous sodium bicarbonate, satu' rated aqueous sodium chloride, dried over Na SO and evaporated leaving a residue. The residue was distilled in a rocking short path distillation apparatus and a product comprising methyl l5-methyl-8,l 1,14- eicosatrienoate was collected at bath temperatures up to 220 at 0.5 to 0.05 mm. The above distillate was dissolved in cyclohexane and chromatographed over 250 g. of silica gel, eluting with l 1. each of 2 /2 percent, 5 percent and percent ethyl acetate in cyclohexane, collecting 100 ml. fractions. Fractions 14 to 18 were evaporated to give 6.80 g. of a residue comprising methyl l5-methyl-8,l 1,14-eicosatrienoate.

H. l5-Methyl-8,l 1,14-eicosatrienoic acid A mixture of 1.3 g. of methyl l5-methyl-8,l1,l4- eicosatrienoic acid, 12.8 ml. of 95 percent ethanol, 1.1 g. of potassium hydroxide and 1.1 ml. of water under a nitrogen atmosphere was heated under reflux for 2 hours, then water and Skellysolve 8" (mixed hexanes) were added. The aqueous and organic layers were separated and the aqueous layer was made acid with 3N hydrochloric acid, then extracted with ether. The ether extract was washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated leaving a residue comprising l5-methyl-8,l 1,14-eicosatrienoic acid. The residue was distilled in a short path tube at bath temperatures of about 180C. and a pressure of about 0.007 mm. The distil late was dissolved in 5 percent ethyl acetate-benzene and chromatographed over 100 g. of acid washed silica gel. Elution with 600 ml. 5%, 500 ml. 10% and 200 ml. 25 percent ethyl acetate in benzene, then with 100 ml. of ethyl acetate. collecting 50 ml. fractions, and evaporation of the eluate fractions gave a first peak of 183 mg., followed by a 448 mg. peak comprising l5-methyl' 8,11,14-eicosatrienoic acid showing one spot on TLC analysis, and having the following NMR absorptions singlet at 628 cps (COOH); multiplet at 322 cps (cis H H); triplet at 167 cps. (diallylic CH and triplet .c\ at 53 cps (Ct'lr).

Preparation 3. 2-Methyl-8,l 1,14-eicosatrienoic acid A. l-Hydroxy-cis,cis,cis-6,9, l 2-octadecatriene A solution of 50 g. of methyi 'y-linolenate in 400 ml. of absolute ether is added dropwise with stirring to a suspension of 25.0 g. of lithium aluminum hydride in 1400 ml. of anhydrous ether under nitrogen. After addition is complete the mixture is stirred and heated under reflux for 6 hrs. The reaction mixture is then cooled with an ice bath, and ethyl acetate is added dropwise with caution to decompose excess lithium aluminum hydride. Water is then added until the inorganic satls separate, and 20 g. of Celite (diatomaceous earth filter aid) is added. The mixture is then filtered through sodium sulfate. and the filtrate is dried over sodium sulfate. The ether solution is then evaporated under reduced pressure, giving 47.26 g. of a residue comprising l-hydroxy-cis,cis,cis-6,9, l 2-octadecatriene and some unchanged starting material.

A solution of 75.0 g. of residue obtained as above is dissolved in 1640 ml. of methanol and stirred under nitrogen, then a solution of 82 g. of potassium hydroxide in m1. of water is added and the mixture is stirred at room temperature (about 23C.) for about 18 hrs. About 50 ml. of water is added to the reaction mixture, and most of the methanol is removed by evaporation under reduced pressure. The mixture is then extracted three times with 500-ml. portions of methylene chlo ride. The methylene chloride extracts are combined and washed with water until the washings are neutral. The methylene chloride solution is then dried over sodium sulfate and evaporated under reduced pressure to give about 69.5 g. of 1-hydroxy-cis,cis,cis-6,9,12- octadecatriene.

B. l-lodo-cis,cis,cis-6,9, l Z-octadecatriene A solution of 28.0 g. of 1-hydroxy-cis,cis.cis-6,9,l2- octadecatriene in 300 ml. of pyridine is cooled in an ice-salt bath and a solution of 45.0 g. of ptoluenesulfonyl chloride in 100 ml. of pyridine is added dropwise over a period of 30 minutes, then the ice-salt bath is removed and the reaction mixture is allowed to stand for 3 hrs. at room temperature. The mixture is then poured into 1 1. of ice and water, and hydrochloric acid is added carefully until the mixture is acidic. The mixture is then extracted 4 times with 200-ml. portions of methylene chloride, keeping the temperature of 0C by adding ice as needed. The methylene chloride extracts are combined and washed with 5 percent hydrochloric acid, then with saturated aqueous sodium bicarbonate, and with water until the washings are neutral. The methylene chloride solution is then dried over sodium sulfate and evaporated under reduced pressure to give about 35 g. of a residue comprising l-hydroxycis,cis,cis-6,9, l 2-octadecatriene p-toluene-sulfonate. The thus obtained p-toluenesulfonate is dissolved in l l. of acetone and stirred under nitroen, then 60 g. of powdered sodium iodide is added and the mixture is stirred and heated under reflux for 4 hrs. The mixture is cooled and filtered to remove precipitated sodium p-toluenesulfonate. The precipitate is washed with 200 m1. of acetone. and the filtrate and the acetone wash are combined and evaporated under reduced pressure to remove most of the acetone. The residue is parti tioned between methylene Chloride and water. The methylene chloride layer is separated and washed with percent aqueous sodium thiosulfate then with water. The methylene chloride solution is dried over sodium sulfate and evaporated under reduced pressure to give about 33.47 g. of a residue comprising l-iodo-cis,cis, cis-6,9,1Z-octadecatriene.

The infrared spectrum in mineral oil shows v 3010, 1680, 1650, 720 cm.

Calcd for C H l: C. 57.76; H, 8.29; l, 33.95

Found: C, 58.30; H. 8.71, l, 32.62

NMR Spectrum in CC] shows peaks centered at 5.4 5(vinyl H). 3.18 5(CH -l protons), 2.7 5

{CH-CH CH protons).

C. 2-Methyl-cis,cis,cis-8,11,14-eicosatrienoic acid A solution of 2.8 g. of sodium in 200 ml. of freshly distilled n-butanol is prepared by adding the sodium in small pieces and stirring under a nitrogen atmosphere until all the sodium is dissolved, then 17.] ml. of diethyl methylmalonate is added and the solution is heated under reflux for 1 hr. The solution is then cooled and a solution of 33.47 g. of l-iodo-cis,cis,cis-6,9,12- octadecatriene in 100 ml. of freshly distilled n-butanol is added. The thus obtained reaction mixture is stirred and heated under reflux in a nitrogen atmosphere for 3 hrs., then the n-butanol is removed by evaporation under reduced pressure. The residue is partitioned be tween methylene chloride and 2N hydrochloric acid. The methylene chloride solution is separated and washed with aqueous sodium bicarbonate, then with water until the washings are neutral, and dried over sodium sulfate. The solvent is removed by evaporation under reduced pressure to give a residue of crude di ethyl ester. The residue is dissolved in 50 ml. of 3A alcohol and added to a solution of 25 g. of potassium hy droxide in 500 ml. of 3A alcohol. The mixture is stirred and heated under reflux in a nitrogen atmosphere for 3 hrs., then ml. of water is added and stirring is continued for an additional hour. The ethanol is then removed by evaporation under reduced pressure, and 500 ml. of ether and 100 ml. of water are added to the residual mixture. The aqueous and the ether layers are separated and the ether layer is twice extracted with 5 percent aqueous sodium hydroxide. The three aqueous extracts are combined and made acid with 2N hydrochloric acid. The acidified mixture is extracted three times with ethyl acetate. The ethyl acetate extracts are washed with water until the washes are neutral. and the water washes are back extracted with ethyl acetate. The ethyl acetate extracts are combined, dried over magnesium sulfate. and evaporated under reduced pressure to give a residue of crude dicarboxylic acid. The thus obtained residue is dissolved in 185 ml. of quinoline and stirred and heated slowly, in a nitrogen atmosphere, to 120C. When the temperature reaches 70C., 5.0 g. of copper eicostrienoic is added in small portions. The temperature is maintained at 120C. for 2 hrs., then the mixture is cooled and poured into excess ice and hydrochloric acid; the mixture should stay acidic. The mixture is extracted 3 times with 500 m1. portions of methylene chloride. The methylene chloride extracts are combined and washed twice with 2N hydrochloric acid, then with water until the washings are neutral, and dried over sodium sulfate. The dried solution is evaporated under reduced pressure to give a residue comprising 2-methyl-cis,cis.cis-8,l 1,14- eicostrieenoic acid.

The NMR spectrum is in agreement with the assigned structure (6 vinyl protons centered at 5.48 4 doubly allylic protons centered at 2.7 5). The material is homogeneous by thin layer chromotography. Preparation 4. l l,15-Dimethyl-8,l 1,14-eicostrienoic acid A. Methyl 4-methyl-3-nonenoate A mixture of 5 g. of l-bromo-3-methyl-2-octene (from Preparation 2, part C), 7 g. of potassium cyanide and 35 ml. of dimethylsulfoxide is stirred and heated under nitrogen for 2.5 hrs. at about 1 10C. The mixture is then poured into water and extracted with ether. The ether extract is washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated under reduced pressure leaving a resi due comprising 4-methyl-3-nonenenitrile. The thus obtained residue is mixed with 45 ml. of 25 percent hydrogen chloride in methanol containing 0.5 ml. of water while cooling with an ice bath, then the ice is allowed to melt and the mixture is stirred for about l8 hours. The mixture is poured into water and extracted with ether. The ether extract is washed with water, aqueous sodium bicarbonate. saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated under reduced pressure leaving a residue comprising methyl 4-methyl-3-nonenoate. The thus obtained residue is dissolved in a mixture of 30 ml. of percent ethanol, 2.5 g. of potassium hydroxide, and 3.0 ml. of water and heated under reflux under nitrogen for about two hours, then water and Skellysolve 3" (mixed hexanes) are added. The aqueous and organic layers are separated and the aqueous layer is made acid with 3N hydrochloric acid, then extracted with ether. The ether extract is dried over sodium sulfate and evaporated under reduced pressure to give a residue comprising 4-methyl-3-n0nenoic acid.

A solution of 10 g. of 4-methyl-3-nonenoic acid in 200 ml. of methanol containing 2 g. of hydrogen chloride is stirred and heated under reflux, under nitrogen, for about 6 hrs, then is allowed to stand about 18 hrs., at room temperature. The mixture is then concentrated under reduced pressure until most of the methanol is removed, poured into ice water, and extracted with ether. The ether extracts are washed with water, then with saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The ether solution is then dried over sodium sulfate and evaporated to give a residue comprising methyl 4-methyl-3-nonenoate.

B. 1-Bromo-4-methyl-3-nonene A solution of 2.5 g. of lithium aluminum hydride in ml. of anhydrous ether is prepared and a solution of 5.0 g. of methyl 4-methyl-3monenoate in 50 ml. of anhydrous ether is added dropwise, with stirring, under nitrogen. The reaction mixture is then heated under reflux for about 6 hrs.. then cooled, and 30 ml. of ethyl acetate is slowly added. Water is added until the inorganic salts separate, then 2 g. of Celite (diatomaceous earth filter aid) is added and the mixture is filtered through sodium sulfate. The filtrate is dried over sodium sulfate and evaporated under redl" 7d pressure to give a residue comprising 4-methyl-3-nonen-l-ol.

A solution of 3 ml. of 4-methyl-3-nonen-1-ol in a mixture of 20 m1. of ether and 1.25 ml. of pyridine under nitrogen is cooled in an ice-salt bath and stirred while 2.7 ml. of phosphorus tribromide is added slowly. The ice bath is removed and the mixture is allowed to warm to room temperature, then is heated under reflux for about 2.5 hrs. The mixture is then cooled in an ice bath while ml of water is added slowly. The layers are separated and the ether layer is washed with water, saturated aqueous sodium bicarbonate, saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated, giving a residue comprising 1-bromo-4- methyl-3-nonenc.

C. Methyl 2,6-dimethyl-2,S-undecadienoate A mixture of 5.0 g. of l-bromo-4-methyl-3-nonene and 6.35 g. of triphenylphosphine in 25 ml. of dry benzene is heated under reflux for 12 hrs., then the mixture is allowed to cool to 25C. and 50 ml. of dry ether and 11 ml. of 15 percent n-butyl lithium in hexane are added. The resulting mixture is stirred for 2 hrs. at C., giving a red solution, then 2.5 g. (2.15 ml.) of methyl pyruvate in 10 ml. of ether is added and the mixture is stirred at room temperature (about 25C.) for 18 hrs. The solvents are then removed by evaporation under reduced pressure and the resulting residue is dissolved in methylene chloride and chromatographed over silica gel. Elution with 5,10 and 20 percent ethyl acetate in cyclohexane and evaporation of the eluate fractions gives a residue comprising methyl 2,6-dimethyl-2,5-undecadienoate.

D. l-Bromo-2,6-dimethyl-2,S-undecadiene Following the procedure of part B of this preparation but replacing methyl 4methyl-3-nonenoate as starting material with a stoichiometrically equivalent amount of methyl 2.6-dimethyl-2,S-undecenoate there is obtained l-bromo-2,6-dimethyl-2,5-undecadiene.

E. l-Chloro-l0,l4-dimethylnonadeca-l0,l3-dien-7- vne A solution of 12.0 g. of l-chlorooct-7-yne in 20 ml. oftetrahydrofuran is added to a mixture of 27 ml. of 3N ethyl magnesium bromide in ether and 50 ml. of tetrahydrofuran. The mixture is stirred and heated under re flux for 30 min. under nitrogen, then 0.45 g. of powdered cuprous chloride is added and heating and stirring is continued for 20 min. A solution of 20.0 g. of lbromo-Z,6-dimethyl-2,5-undecadiene in 15 ml. of tetrahydrofuran is added and the mixture is heated under reflux for 10 hrs. then allowed to stand for about 18 hrs., and poured into saturated amount aqueous ammonium chloride and ether. The mixture is filtered and the ether solution is separated, washed with water, dried over sodium sulfate, and evaporated to leave a residue comprising l-chlorol O, 1 4-dimethylnonadecal 0, l 3- dien-7-yne.

F. -Chlorol0, l4-dimethylnonadeca-7,10, l3-triene A mixture of 5.0 g. of l-chloro-10,l4- dimethylnonadeca-IO, l 3-dien-7-yne, 500 mg. of5 percent palladium-barium sulfate catalyst and 40 ml. of pyridine is shaken under hydrogen for about 2 hrs. (until the uptake of hydrogen practically ceases). The mixture is then filtered, diluted with water, and ex tracted with ether. The ether extract is washed with water, dilute hydrochloric acid, and aqueous sodium bicarbonate. then is dried over sodium sulfate and evapo rated to leave a residue comprising l-chloro-l0,l4- dimethylnonadeca-7, l 0, l 3-triene.

G. l l,l5-Dimethyl-8,l 1,14-eicosatrienoic acid A mixture of 10.0 g. of l-chloro-l0,l4-dimethylnonadeca-7,l0,l3-triene. 10 g. of potassium cyanide and 50 ml. of dimethyl-sulfoxide is heated under nitrogen at 1 15 with stirring for about 2.5 hrs., then is allowed to cool, poured into water, and extracted with ether. The ether extract is washed with water. dried over sodium sulfate, and evaporated. The residue is stirred with ml. of 25 percent hydrogen chloride in methanol while cooling with ice. The ice is allowed to melt and stirring is continued for a total time of about 20 hrs., then water is added and the mixture is extracted with ether. The ether extract is washed with wa ter, dried over sodium sulfate, and evaporated. The residue is distilled in a rocking short-path distillation apparatus at about 0.005 mm. to give a distillate comprising methyl 1 l,15-dimethyl8,1 1,14-eicosatrienoate. The thus obtained methyl ester is dissolved in a mixture of 75 ml. of percent ethanol and 6.0 g. ofpotassium hy droxide in 6 ml. of water, and the mixture is heated under reflux for two hours, then ml. of water is added and 150 ml. of ether. The water layer is separated, made acid with 3N hydrochloric acid, and extracted with ether. The ether extracts are washed with water, dried over sodium sulfate and evaporated to give a residue comprising 11,l5-dimethyl-8 1 1,14- eicosatrienoic acid, which can be further purified by distillation in a short-path tube at a pressure of about 0.005 mm.

Preparation 5. 8,12-Dimethyl-8,l 1,14-eicosatrienoic acid A. 3-Nonenoic acid A mixture of5 g. of l-bromo-Z-octyne, 7 g. of potassium cyanide and 35 ml. of dimethylsulfoxide is stirred and heated under nitrogen for about 2.5 hrs. at reflux temperature. The mixture is then poured into water and extracted with ether. The ether extract is washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated under reduced pressure leaving a residue comprising 3- nonynenitrile. The thus obtained residue is mixed with 45 ml. of 25 percent hydrogen chloride in methanol containing 0.5 ml of water while cooling in an ice bath. The ice is allowed to melt and the mixture is stirred for about 18 hrs., then is poured into water and extracted with ether. The ether extract is washed with water, aqueous sodium bicarbonate, and saturated aqueous sodium chloride, dried over sulfate, and evaporated under reduced pressure leaving a residue comprising methyl 3-nonynoate. A mixture of the thus obtained methyl 3-nonynoate, 500 mg. of 5 percent palladiumbarium sulfate catalyst and 40 ml. of pyridine is shaken under hydrogen for about 2 hrs., until the uptake of hydrogen practically ceases. The mixture is then filtered, diluted with water, and extracted with ether. The ether extract is washed with water, dilute hydrochloric acid. and aqueous sodium bicarbonate, then is dried over so dium sulfate and evaporated to leave a residue comprising methyl 3-nonenoate.

The residue of methyl 3-nonenoate is dissolved in a mixture of 30 ml of 95 percent ethanol, 2.5 g. of potassium hydroxide, and 3 ml. of water and heated under reflux under nitrogen for about 2 hrs., then water and Skellysolve B" (mixed hexanes) are added. The aqueous layer is separated and made acid with 3N hydrochloric acid. then extracted with ether. The ether extract is dried over sodium sulfate and dried under reduced pressure to give a residue comprising 3-nonenoic acid.

B. 4-Decen-2-one A mixture of 22 g. of 3-nonenoic acid and l()() ml. of thionyl chloride is stirred at room temperature for about an hour, then 150 ml. of l:l ether-benzene mixture is added. The solvents are removed by evaporation under reduced pressure, then another l50 ml. of lzl ether benzene mixture is added to the residue, and re moved by evaporation under reduced pressure, leaving a residue comprising 3-nonenoyl chloride. This residue is then dissolved in 30 ml. of benzene.

A mixture of 68 ml. of 3M methyl magnesium bromide in ether and 70 ml. of ether is cooled in an ice bath while 18.3 g. of dry cadmium chloride is added in portions. The ice bath is removed and the mixture is heated under reflux for about 45 minutes, then most of the ether is removed by evaporation under reduced pressure and 70 ml. of benzene is added, followed by slow addition of the 3-nonenoyl chloride in benzene solution prepared above. The thick, white mixture is heated under reflux for one hour, then is cooled in an ice bath and 60 ml. of ice water is added, followed by enough 1N sulfuric acid to give two clear phases. The organic layer is separated and washed with water, saturated aqueous sodium bicarbonate, dried. and distilled through a Vigreaux column to give a distillate comprising 4-decen-2-one.

C. 3-Hydroxy-3-methylundec-5-en-l-yne A mixture of 45.5 g. of lithium acetylide-ethylene diamine, 200 ml. of dry tetrahydrofuran, and 200 ml. benzene at 35C. is stirred under nitrogen while 50 g. of 4-decen-2-one in 50 ml. of benzene is added slowly. The mixture is then stirred for about 2.5 hrs., and 130 ml. of water is added slowly. The mixture is heated under reflux for one hour, cooled, and extracted with ether. The ether extract is washed with water, 1N hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride, then is dried and evaporated under reduced pressure. The residue is distilled through a Vigreaux column giving a distillate comprising 3-hydroxy-3-methylundec-S-en-lyne.

D. 3-Hydroxy-3-methyl-l,5-undecadiene A mixture of 20.0 g. of 3-hydroxy-3-methyl undec-lyne, 200 ml. of pyridine, and 500 mg. of Spercent palladium on barium sulfate is shaken in hydrogen at an initial pressure of 45 lb./sq. in. The hydrogenation is stopped when the calculated amount for one mole uptake per mole of compound has been absorbed. The mixture is poured into water and extracted with ether. The ether extract is washed with water, dilute hydrochloric acid, aqueous sodium bicarbonate, dried, and evaporated under reduced pressure to give a residue which is distilled through a Vigreaux column to give a distillate comprising 3 hydroxy-3-methyll ,5- undecadiene.

E. l-Bromo-3-methyl-2,5-undecadiene In an ice-salt bath 25 ml. of 48percent hydrobromic acid is saturated with hydrogen bromide by bubbling through for 5 to l0 min., then g. of 3-hydroxy-3 methylundec'l-ene is added slowly, with stirring. After an additional min. of stirring benzene is added, then the benzene layer is separated, washed with ice-water, saturated aqueous sodium bicarbonate, saturated sodium chloride, dried, and evaporated under reduced pressure giving a residue which is distilled through a Vigreaux column to give a main fraction of distillate comprising l-bromo-3-methyl-2,5-undecadiene.

F. l-Bromo-4-methyl-3,o-dodecadiene Following the procedure of Preparation 4, part A, but replacing l-bromo-3-methyl-2octene as starting material with l-bromo-3-methyl-2,S-undecadiene is productive of methyl 4-methyl 3,o-dodecadienoate.

Following the precedure of Preparation 4, part B, but replacing methyl 4-methyl-3-nonenoate as starting material with methyl 4-methyl-3,b-dodecadienoate is pro ductive of 1-bromo-4-methyl-3,o-dodecadiene.

G. Methyl 2,6-dimethyl-2,5,8-tetradecatrienoate Following the procedure of Preparation 4, part C, but replacing l-bromo'4-methyl-3nonene as starting material with a stoichiometrically equivalent amount of l-bromo-4-methyl-3,6-dodecadiene is productive of methyl 2,6-dimethyl-2,5,8-tetradecatrienoate.

H. l-Bromo-2,6-dimethyl-2,5,8-tetradecatriene Following the procedure of Preparation 4, part B, but replacing methyl 4-methyl3-nonenate as starting material with a stoichiometrically equivalent amount of methyl 2,6-dimethyl-2,5, S-tetradecatrienoate is procuctive of l-bromo2,6-dimethyl-2,5, 8- tetradecatriene.

l. 8,l2-Dirnethyl-8,l l,l4-eicosatrienoic acid A solution of 22 g. of 1-bromo-2,6-dimethyl-2,5,8- tetradecatriene, and 20 g. of methyl o iodohexanoate in 60 ml. ofa 1:1 mixture of anhydrous ether and benzene is added to 2.5 g. of magnesium in 30 ml. of ether over a period of 5 min., a crystal of iodine and 20 mg. of mercuric chloride are introduced, and the mixture is heated under reflux under nitrogen for about 3 hr., then an additional 20 mg. of mercuric chloride is introduced and heating is continued for a further 3 hrs. The reaction mixture is then cooled to 5l0C. and treated with dilute hydrochloric acid. The upper layer is then separated and the organic layer is extracted with ether. The extracts are combined and washed with aqueous sodium bisulfite, saturated aqueous sodium bicarbonate and dried over sodium sulfate, then evaporated under reduced pressure to give a residue. The residue is distilled at a pressure of about (J.l mm. After collecting some unchanged starting material a distillate fraction comprising methyl 8,l2-dimethyl 8,l l,l4- eicosatrienoate is collected.

A solution of 5 g. of the thus obtained methyl ester in a mixture of ml. of percent ethanol and 5.0 g. of potassium hydroxide in 5 ml. of water is heated under reflux under nitrogen for about 2 hrs., then l50 ml. of water and ml. of ether are added. The water layer is separated and made acid with 3N hydrochloric acid. and extracted with ether. The ether extracts are washed with water, dried over sodium sulfate, and evaporated to give a residue comprising 8, l 2-dimethyl- 8, l l,l4-eicosatrienoic acid.

Preparation 6. 3-Methyl-8,l 1,14-eicosatrienoic acid A. Cis,cis,cis 6,9, l 2-octadecatrienol A solution of 50 g. of methyl y-linolenate in 400 ml. of absolute ether is added dropwise with stirring to a suspension of 250 g. of lithium aluminum hydride in 1400 ml. of ether under nitrogen. Stirring is continued and the mixture is heated under reflux for 6 hrs. The mixture is then cooled in an ice bath and stirred while 300 ml. of ethyl acetate is added dropwise. followed by addition of water until the inorganic salts separate.

Next, 20 g. of Celite (diatomacoeous earth filter aid) is added and the mixture is filtered. The filtrate is dried over sodium sulfate and evaporated under reduced pressure to give 47.26 g. ofa residue comprising cis.cissis-6,9,12-octadecatrienol.

B. Cis,cis cis-6.9. l 2-octadecatrienal A solution of 20 g. of cis,cis.cis-6.9.l2- octadecatrienol in 400 ml. of acetone is cooled to C. and 40 ml. of Jones reagent (10.3 g. Cro 30 ml. H O, 8.7 ml. concentrated H SO is added dropwise over a period of 10 min. while stirring. The reaction mixture is stirred for an additional min. at 10C. then the excess Jones reagent is destroyed by addition of 25 ml. of isopropanol. The reaction mixture is diluted with water and extracted several times with ether. The ether extracts are combined and washed with aqueous sodium bicarbonate, then water, and dried over sodium sulfate, then evaporated under reduced pressure to give a residue comprising cis,cis,cis- 6,9,12-octadecatrienal.

C. Cis.cis,cis-7,l0,l3-n0nadecatrien-2-ol A solution of 26 g. of cis.cis,cis-6,9,l2- octadecatrienal in 200 ml. of absolute ether is added slowly with stirring. to a solution of 0.15 moles of methyl magnesium bromide in 200 ml. of ether (50 ml. of 3N methyl magnesium bromide in ether diluted with absolute ether to 200 ml.) while heating under reflux under nitrogen. Heating is continued for an hour after addition of the aldehyde is completed, then the reaction mixture is cooled in an ice bath and 200 ml. of 1N hydrochloric acid is added with caution. The ether layer is separated. washed with aqueous sodium bicarbonate, dried over sodium sulfate, and evaporated under reduced pressure to give a residue comprising cis,cis,cis-7,l0,13-nonadecatrien-2-ol.

D. 2-lodo-cis,cis,cis-7,10,1 3-nonadecatriene A solution of 28 g. of cis,cis.cis-7,10,13-nonadecatrien-Z-ol in 300 ml. of pyridine is cooled in an ice-salt bath and stirred while a solution of 45.0 g. of ptoluenesulfonyl chloride in 100 ml. of pyridine is added over a period of 30 min., then the ice-salt bath is removed and the reaction is allowed to proceed for 3 hrs. at room temperature. The reaction mixture is then poured into 1000 ml. of ice and water, and hydrochloric acid is added carefully until the mixture is acidic. The mixture is extracted with 4 200-ml. portions of methylene chloride. adding ice if needed to keep the temperature at 0C. The methylene chloride solutions are combined and washed with ice cold 5 percent aqueous hydrochloric acid, then with cold saturated aqueous sodium bicarbonate, and finally with water until the washings are neutral. The methylene chloride solution is then dried over sodium sulfate. and evaporated under reduced pressure to give a residue comprising cis,cis,cis-7,l0,lBmonadecatrien-Z-ol p-toluensulfonate. The thus obtained p-toluenesulfonate is dissolved in 5000 ml. of acetone, 60 g. of powdered sodium iodide is added. and the mixture is stirred and heated under reflux, under nitrogen, for 4 hours. Next the mixture is cooled and filtered to remove precipitated sodium p-toluenesulfonate. The filtrate is evaporated under reduced pressure and the thus obtained residue is dissolved in methylene chloride and water. The methylene chloride solution is separated and washed with water, then with aqueous 5 percent sodium thiosulfate, again with water, then is dried over sodium sulfate and evaporated under reduced pressure to give a residue comprising 2-iodocis,cis,cis-7, l0, 1 3-nonadecatriene.

E. 3-Methyl-8,l l,l4-eicosatrienoic acid A solution of sodium butoxide is prepared by adding 2.8 g. of metallic sodium in small pieces to 200 ml. of freshly distilled n-butanol under nitrogen while stirring. then 15.3 ml. ofdiethyl malonate is added and the mixture is heated under reflux for 1 hour. The mixture is cooled. and a solution of 34 g. of 2-iodo-cis,cis.cis 7,10,13-nonadecatriene in 200 ml. of freshly distilled n-butanol is added. The resulting reaction mixture is heated under reflux under nitrogen with stirring for 3 hrs, then the n-butanol is removed by distillation under reduced pressure. The thus obtained residue is partitioned between methylene chloride and 2N hydrochloric acid. The methylene chloride solution is separated, washed with aqueous sodium bicarbonate, then with water until the washings are neutral, dried over sodium sulfate, and evaporated under reduced pressure to give a residue. The residue is dissolved in 50 ml. of percent alcohol and added to a solution of 25 g. of potassium hydroxide in 500 ml. of 95 percent ethanol. then is stirred and heated under reflux. under nitrogen, for 3 hrs., at which time 10 ml. of water is added and heating is continued for one more hour. The ethanol is then removed by distillation under reduced pressure and 500 ml. of ether and ml. of water are added. The aqueous layer is separated and the ether is extracted with 5 percent aqueous sodium hydroxide. The aqueous layers are combined and made acid with 2N hydrochloric acid, then are extracted three times with ethyl acetate. The ethyl acetate extracts are combined and washed with water until the washes are neutral, dried over magnesium sulfate and evaporated under reduced pressure to give a residue. The residue is dissolved in 200 ml. of quinoline and stirred and heated under nitrogen. The mixture is slowly heated (30 min.) to C. When the temperature reaches 70C. 5 g. of copper powder is added in small portions. The temperature is maintained at 120C. for 2 hrs, then the mixture is cooled and poured into excess ice and hydrochloric acid. The mixture should stay acidic. The mixture is extracted with 3 500m]. portions of methylene chloride. The extracts are combined and washed twice with 2N hydrochloric acid, then with water until the aqueous washings are neutral, dried over sodium sulfate, and evaporated under reduced pressure to give a residue comprising 3-methyl-cis,cis,cis-8,l 1,14- eicosatrienoic acid.

EXAMPLE 1.

Racemic 7-[3oz,5a-peroxy 2B-(2-octenyl)cyclopentla-yl ]heptanoic acid (9,1 l-peroxyl 4-prostenoic acid) (2) and racemic 7-l3a,5a-peroxy-2B-(3-hydroperoxy- 1-octenyl)cyclopent-la-yl]heptanoic acid (9,1 lperoxy-l S-hydroperoxy-l 3-prostenoic acid) (3).

A solution of 1.0 g. of bishomo-y-linolenic acid (cis.- cis,cis-8.l l14-eicosatrienoic acid) in 4.5 ml. of 1N aqueous sodium hydroxide is diluted to 100 ml. with water, then 40 mg. of hematoporphyrin hydrochloride and 25 mg. of 2,6-di-t-butyl-p-cresol are added and the mixture is stirred in an atmosphere of oxygen while ir radiating with external daylight fluorescent tubes placed close to the glass reaction vessel. After about 40 hr. an additional 40 mg. of hematoporphyrin hydrochloride is added to replace that which has been bleached. After a total of about 75 hrs. of stirring and irradiation about lot] ml. of oxygen has been absorbed. The solution is then acidified with dilute hydrochloric acid and extracted with ether. The ether solution is separated and washed with water. then with saturated aqueous sodium chloride. The washed ether solution is then dried over anhydrous sodium sulfate, filtered. and evaporated to leave a nearly colorless oil. comprising a mixture of racemic 7-[3oz,5a-peroxy-2B-(Z-octenyl)- cyclopent-lwyl] heptanoic acid (2) racemic 7-! 30,50:- peroxy-2B-( 3-hydroperoxyl -octenyl )cyclopentla-yllheptanoic acid (3 and bishomo-y-linolenic acid l The thus obtained mixture is dissolved in a small amount of ethyl acetate and chromatographed on 100 g. of acid-washed silica gel, eluting with ethyl acetate followed by ethyl acetate containing increasing per centages of methanol. Unchanged bishomo-y-linoienic acid linolenic eluted first, followed by racemic 7- [3a,Sa-peroxy-2B(2octenyl)cyclopent-la-yl1- heptanoic acid (2) and racemic 7-[3a,5aperoxy-2B- (3 -hydroperoxyl -octeny )cyclopent-l wyl lheptanoic acid (3). The racemic 7 [3a,5a-peroxy 2B-(2-octenylcyclopentla-yllheptanoic acid (2) and racemic 7- [3a,50z peroxy-2B-( 3-hydroperoxyl octenyl cyclopent-la-yl] heptanoic acid (3) obtained by evaporation of the chromatogram eluates can each be used without further purification or can be further purified by reversed phase partition chromatography or countercurrent distribution.

EXAMPLE 2.

Racemic 7-[3(x,5a peroxy-2B-(2 octenyl)cyclopentla-yllheptanoic acid (2) and racemic 7-[3a,5aperoxy-2/3-( 3-hydroperoxyl -octenyl )-cyclopent l oryllheptanoic acid (3).

A solution of 3.06 g. (l mmoles) of bishomo-ylinolenic acid l in 50 ml. of benzene is stirred with 7.25 g. mmoles) of the endoperoxide of 9.10 diphenylanthracene and the mixture is slowly warmed until the endoperoxide begins to decompose and liberate singlet oxygen. Stirring is continued at this temperature until decomposition of the anthracene endoperoxide is complete. The mixture is then concentrated to a small volume and chromatographed on 300 g. of acid washed silica gel. The chromatogram column is eluted first with l:l benzene-ethyl acetate, then ethyl acetate, and finally 5l 5 percent methanol in ethyl acetate. and the eluate fractions are evaporated to give first 9,10 diphenyl anthracene. followed by bis-homo-ydinolenic acid (1), racemic 7-[3a,5a peroxy-2B-(2-octenyl)- cyclopent-la-yllheptanoic acid (2) and racemic 7- [3a,5a-peroxy-2B-( 3-hydroperoxyl -octenyl )cyclopent-la-yHheptanoic acid (I 3). The products are suffi ciently pure for further use. or can be further purified as described above.

EXAMPLE 3.

Racemic 7-[3oz,5a-peroxy"2;3(2-octenyl)cyclopentla-yl]heptanoic acid (2) and racemic 7-[ 301,50: peroxy-2/3( 3-hydroperoxyl -octeny] )cyclopentl ayllheptanoic acid (3).

The adduct of ozone and tri-(p-tolyl)phosphite moles) in methylene chloride at -70 C. is prepared as described by QE. Thompson. J. Am. Chem. Soc., 83, 845 l96l To this cold solution is added a solution of 3.06 g. (H) mmoles) of bishomo-y-linolenic acid in 25 ml. of cold methylene chloride. The solution is then stirred and allowed to warm slowly to room tempera ture. after which stirring is continued for about 30 min utes, then the solution is concentrated to a small volume and chromatographed on 300 g. of acid-washed silica gel. Elution with a l:l mixture of benzene-ethyl acetate followed by ethyl acetate and finally 5-l5 percent methanol in ethyl acetate and evaporation of the eluates gives residues comprising bishomo-y-linolenic acid (I). racemic 7[3a.5aperoxy-2B-(2-octenyl)- cyclopcnt-lcx-yl1heptanoic acid (2) and racemic 7- l3a,Saperoxy-2B-( 3--hydroperoxyl -octenyl )cyclopentla-yl lheptanoic acid (3). The thus-obtained products are sufficiently pure for use in further transformations, or can be further purified as described above.

EXAMPLE 4.

Racemic 7-[3o.5a-peroxy-2B-(2-octenyl)cyclopentlwyllheptanoic acid (2) and racemic 7-[3a,5aperoxy-2fi-( 3-hydroperoxyl -octenyl )cyclopentl ayllheptanoic acid (3 The effluent gases resulting from the electrodeless discharge of radio frequency current through oxygen in an apparatus as described by E. J. Corey, J. Am. Chem. Soc. 86, 388] (196 are bubbled through a solution of 300 mg. of bishomoy-linolenic acid in 25 ml. of chlorobenzene at 25 containing 50 mg. of 2,6-di-tbutyl-p'cresol for a period of about 48 hrs. The solution is then concentrated under diminished pressure. and the thus obtained residue is dissolved in a small amount of ethyl acetate and chromatographed over 50 g. of acid washed silica gel. On elution with ethyl acetate containing increasing amounts of methanol and evaporation of the eluates there is obtained first racemic 7 [3a,5a-peroxy-2B4 2-octenyl )cyclopentl B- yllheptanoic acid (2) and then racemic 7-[3a,5aperoxy=2[3( 3-hydroperoxyl -octenyl )-cyclopentl B yllheptanoic acid (3). The products, which are sufficiently pure for use in subsequent transformations, can be further purified as described above.

EXAMPLE 5.

Racemic 7-[3a,50z-peroxy-2B(2-octenyl)cyclopentloc-yllheptanoic acid (2) and racemic 7-[30z,5aperoxy-2fi( 3-hydroperoxy l octenyl )cyclopentl ayl]heptanoic acid (3).

A solution of 3.06 g. of bishomo-y-linolenic acid in 300 ml. of methanol is cooled to 10 C. and stirred, then 19.2 ml. of 30 percent hydrogen peroxide is added, followed by 145 ml. of 1 .03M sodium hypochlorite added over a period of minutes. The solution is then diluted with water, made acid by addition of dilute aqueous hydrochloric acid, and extracted with ether. The ether layer is separated, washed with water then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated to give a residue comprising racemic 7-[ 3a,5a-pcroxy-2B-( Z-octenyl )cyclopentlor-yllheptanoic acid (2) and racemic 7-l3oa5aperoxy-2B-( Thydroperoxyl octenyl )cyclopentl 01- yl]-heptanoic acid (3). The thus obtained residue is chromatographcd over 300 gv of acid washed silica gel following the procedure of Example 1 to give racemic 71 3t1,5a-pcroxy-Z[3-( 'l-octenyl )cyclopcntl ayl lheptanoic acid (2) and racemic 7[ 3a,5a-peroxy-2B- (3-hydroperoxyl octenyl )cyclopentl myllheptanoic acid (3) which can each be used directly for subsequent transformations or can he further purified as de scribed above.

EXAMPLE 6.

Race mic 7-[ 301,5 a-peroxy-2B-( 2-octenyl )-cyclopent la-yl1heptanoic acid (2) and racemic 7430:50- peroxy 2/3-( 3a-hydroperoxyl -octenyl )cyclopentl ayllheptanoic acid (3).

A solution of 3.06 g. of bishomo-y-linolenic acid in 25 ml. of ethanol containing 2 g. of potassium hydroxide and 5 ml. of benzyl cyanide is treated dropwise with 5 ml. of 30 percent hydrogen peroxide at room temperature. When the oxygen evolution has ended the solution is diluted with water, made acid with dilute aqueous hydrochloric acid, and concentrated under diminished pressure until the ethanol is removed. The aqueous residue is then extracted with ether and the ether extract is washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated under reduced pressure to give a residue comprising racemic 7-[3a,5a-peroxy-2B-(2- octenyl)cyclopent-la-yl]heptanoic acid (2) and racemic 7-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyl)cyclopent-la-yl]heptanoic acid (3). The products can be separated by chromatography over 300 g. of acid washed silica gel following the procedure of Example 1.

EXAMPLE 7.

Racemic 8-[3a,5a-peroxy-2B-(2-octenyl)-cyclopentla-ylloctanoic acid (2) and racemic 8-[3a,5a-peroxy- 2B4 3-hydroperoxyl -octenyl)cyclopentlayl]octanoic acid (3 Following the procedure of Examples 1 to 6, but substituting as starting material cis,cis,cis-9,l2,l5- heneicosatrienoic acid in place of bishomo-y-linolenic acid is productive of racemic 8-[3a,5a-peroxy-2B-(2- octenyl)cyclopent-la-yl]octanoic acid (2) and racemic 8-[3a,5a-peroxy-2B-(3-hydroperoxy-l-octenyl)- cyclopent-la-ylloctanoic acid (3), which can be isolated and purified as described in the above Examples.

Following the procedure of Examples 1 to 6, but substituting for bishomo-y-linolenic acid as starting material the following acids: 7,l0,l3-hexadecatrienoic acid,

6,9,1 2'octadecatrienoic acid, 9,12.15-octadecatrienoic acid (linolenic acid), 7.10.13-nonadecatrienoic acid, 4,7,10 l3-nonadecatetraenoic acid,

5,8,1 l-eicosatrienoic acid,

5.8,] l,l4-eicosatetraenoic acid (arachidonic acid), 8,! l,l4.l7-eicosatetraenoic acid,

7, l 0,] 3-docosatrienoic acid,

7,10, l 3, l fi-docosatetraenoic acid,

l5-methyl-8,l l,l4-eicosatrienoic acid, l6-methyl-8.l l. l 4-eicosatrienoic acid,

I l.l5-dimethyl-8,l l,l4-eicosatrienoic acid, 8,l2-dimethyl-8.l l,l4-eicosatrienoic acid, and 16.16-

dimethyl-8.ll,l4-eicosatrienoic acid, there are obtained: racemic 6-[3a,5a-peroxy-2B-(2-pentenyl)cyclopentla-yl1hexanoic acid (2) and racemic 6-[3a,5a-peroxy- 2H4 3-hydroperoxy-l-pentenylJcyclopent-10:- yl]hexanoic acid (3).

racemic 5[ 3a,5a-peroxy-2B-(2-octenyl)cyclopent-1ayllpentanoic acid (2) and racemic 5-[3a,5a-peroxy- 2B-( 3-hydroperoxy-l -octenyl )-cyclopentl ayllpentanoic acid (3).

26 racemis 8-[3a,5a-peroxy-2B-(2-pentenyl)cyclopentla-yl]octanoic acid (2) and racemic 8-[ 3a,5a-peroxy- 2{3-( 3-hydroperoxyl -pentenyl )-cyclopentl aylloctanoic acid (3), racemic 6-[ 3oz,5oz-peroxy-2-octenyl )cyclopent- I my] hexanoic acid (2) and racemic 6-[3a,5a-peroxy-2B 3- hydroperoxyl -0ctenyl )-cyclopent loz-hexanoic acid (3). racemic 6-! 3a,5a-peroxy-2B-( 2-octenyl )cyclopentlalyll-4-hexenoid acid (2) and racemic 6-[3a,5aperoxy-2B-( 3-hydroperoxyl -octenyl)-cyclopentl ayl]-4-hexenoic acid (3 racemic 4-[3a,5 a-peroxy-2B-( 2-undecenyl )cyclopentla-yll-butanoid acid (2) and racemic 4-[3a,5aperoxy-2B-( 3-hydroperoxyl -undecenyl )-cyclopentla-yl]butanoic acid (3), racemic 7-[3a,5a-peroxy-2B-(2-octenyl)cyclopentlayll-S-heptenoic acid (2) and racemic 7-[3a,5aperoxy-2B-( 3-hydroperoxyl -octenyl-cyclopent-l ayl1- S-heptenoic acid (3), racemic l0-[3a,5a-peroxy-2B-(2-pentenyl)cyclopentlayl]-8-decenoic acid (2) and racemic l0-[3a,5aperoxy-2B-( 3-hydroperoxyl-pentenyl )-cyclopentl ayl]-8-decanoic acid, racemic 6-[3a,5a-peroxy-2B-(2-undecenyl)cyclopentloz-yll-hexanoid acid (2) and racemic 6-[3a,5aperoxy-2,B-( 3-hydroperoxyl -undecenyl )-cyclopentla-yllhexanoic acid (3). racemic 9-[ 301,5 a-peroxy-2B-( 2-octenyl )cyclopentl ayl]-7-nonenoic acid (2) and racemic 9-[3a,5a-peroxy- 2B-( 3-hydroperoxyl -octenyl )-cyclopentl a-yl -7- nonenoic acid (3), racemic 7[3a,5a-peroxy-2B-(3-methyl-2-octenyl)- cyclopent-la-yllheptanoic acid (2) and racemic 7- [3a,5oz-peroxy-2B-( 3-hydroperoxy-3-methyll octenyl)cyclopent-la-yllheptanoic acid (3), racemic 7-[3a,5a-peroxy-2B(4-methyl-2-octenyl)cyclopentla-yH-heptanoid acid (2) and racemic 7 [3a,5aperoxy-2B-( 3-hydro-peroxy-4-methyll -octenyl cyclopentl a-yl]-heptanoic acid (3 racemic 7-(3a,5a-peroxy-3B-methyl-2B(3-methyl-2- octenyl)-cyclopent-la-ylI-heptanoic acid (2) and racemic 7-[3a,5a-peroxy-3B-methyl-2543-hydroperoxy-3- methyll-octenyl )cyclopentl a-yl ]heptanoic acid (3 racemic 7-[ 3a,5a-peroxyl fi,2a-dimethyl-2B-( 2- 0cteny1)-cyclopent-Ia-yHheptanoic acid (2) and racemic 7-[ 3a,5a-peroxyl fi,2a-dimethyl-2B-( 3- hydroperoxyl-octenyl)cyclopentl a-yl ]heptanoic acid (3), and racemic 7-[ 3a,5a-peroxy-2B( 4,4-dimethyl-2- octenyl)cyclopent-la-yll-heptanoic acid (2) and racemic 7-[3a,5a-peroxy-2fi-(3-hydroperoxy-4,4- dimethyll-octenyl )-cyclopentla-yl ]-heptanoic acid )7 EXAMPLE 8.

Racemic 7-{ 301,5 a-peroxy-2B-( 3-hydroperoxyl octenyl )cyclopentla-yl ]heptanoie acid (3 A solution of 2.0 g. of racemic 7-[3a,5a-peroxy-2B- (2-octenyl)cyclopent-la-yl]heptanoic acid (2) in 9.0 ml. of IN aqueous sodium hydroxide is diluted to ml. with water, then 40 mg. of hemotoporphyrin hydrochloride and 25 mg. of 2,6-di-t-butyl-p-cresol are added and the mixture is stirred in an atmosphere of oxygen while irradiating with external daylight fluorescent tubes placed close to the glass reaction vessel. After about 40 hr. an additional 40 mg. of hematoporphyrin hydrochloride is added to replace that which has been bleached. After a total of about 75 hr. of stirring and irradiation the solution is acidified with dilute hydrochloric acid and extracted with ether. The ether solution is separated and washed with water, then with saturated aqueous sodium chloride, and dried over anhydrous sodium sulfate. The ether solution is then evaporated to give an oil which is dissolved in a small amount of ethyl acetate and chromatographed on 200 g. of acid washed silica gel. Elution with ethyl acetate containing increasing percentages of methanol and evaporation of the eluates gives racemic 7-[3a,5aperoxy 2B-( 3-hydroperoxyl -octenyl) cyclopentl ayl]-heptanoic acid (3 which can be further purified by reversed phase partition chromatography or countercurrent distribution.

Following the procedure of Example 8, but substituting for racemic 7-[3a,5a-peroxy-2B(2-octenyl)cyclopent-lor-yllheptanoic acid (2) as starting material other acids of formula 2, for example racemic 8- [3a,5a-peroxy-2B-( 2-octenyl )cyclopentla-ylloctanoate (2) and the other acids of formula 2 named following Example 7, is productive of the cone sponding acids of formula 3, for example racemic 8- [3a,5a-pe roxy-2l3-( 3-hydroperoxyl octenyl)cyclopent-la-yl]octanoate (3) and the other acids of formula 3 named following Example 7.

Following the procedures of Examples 2 through 6, but substituting for bishomo-y-linolenic acid as starting material two equivalents of an acid of formula 2 is productive of the corresponding acid of formula 3, which can be isolated as shown above.

EXAMPLE 9.

Racemic 7-[ 304,5 a-dihydroxy-2B-( 3-hydroxyl octenyl )cyclopent-la-yllheptanoic acid (racemic prostaglandin F a) (4).

To a solution of l.0 g. of racemic 7-[3a,5a-peroxy- 2/3-( 3-hyd roperoxyl -octenyl )cyclopent l ayl]heptanoate (3) in 25 ml. of isopropanol is added a solution of 1.0 g. of sodium borohydride in 5 ml. of 0. lN aqueous sodium hydroxide. The mixture is stirred for about an hour at room temperature, then is made acid with dilute hydrochloric acid and diluted with water. The mixture is then concentrated under reduced pressure until the isopropanol is removed, and the aqueous residue is extracted with ethyl acetate. The ethyl acetate extract is washed with water, then saturated aqueous sodium chloride, dried, and evaporated under reduced pressure. The residue is dissolved in a small amount of ethyl acetate and chromatographed over lOO g. of acid washed silica gel. The chromatogram is eluted with ethyl acetate containing increasing percentages of methanol and the eluate fractions are evaporated. The thus obtained residues are analyzed by thin layer chromatography (TLC), using silica gel or silver nitrate impregnated silica gel as adsorbent and developing with a mixture of parts by volume of acetic acid, 10 parts of methanol, and 80 parts of chloroform. The residues showing an R; value of about 0.52 comprise racemic 7-l 3a,5a-dihydroxy-2B-(3-hydroxyl-octenyl )cyclopentl a-yl]heptanoic acid.

Following the procedure of Example 9, but substituting for racemic 7-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyl)cyclopent-la-yl]heptanoic acid (3) as starting material other acids of formula (3), for example:

racemic 8-[3a,5a-peroxy-2B-(3-hydroperoxy-1- octenyl)-cyclopent-la-ylloctanoic acid (3),

racemic 6-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl pentenyl )-cyclopentla-yllhexanoic acid (3 5 racemic S-l3a,5a-peroxy-2B(3-hydroperoxy-loctenyl)-cyclopentla-yllpentanoic acid. racemic 8-l 3a,5a-peroxy-2B-( 3-hydroperoxy- 1 pentenyl )-cyclopentla-ylloctanoic acid (3 racemic o-l 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyl)-cyclopent-la-yllhexanoic acid (3 racemic 6-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyU-cyclopentla-yl]-4-hexenoic acid (3), racemic 4-[ 301,5 a-peroxy-2B-( 3-hydroperoxyl undecenyl )cyclopentl a-yllbutanoic acid (3 racemic 7-[3a,5a-peroxy-2B-(3-hydroperoxy-loctenyl)-cyclopent-1a-yl]-5-heptenoic acid (3 racemic 10-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl pentenyl)cyclopent-la-yll-8-decenoic acid (3), racemic 6-[ 3a,5a-peroxy-2/3-( 3-hydroperoxyl undecenyl)-cyclopentla-yllhexanoic acid (3), racemic 9-[ 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyl)-cyclopent-1a-yl1-7-nonenoic acid (3), racemic 7-[ 3a,5a-peroxy-2B-( 3-hydroperoxy-3-methyll-octenyl) cyclopent-la'yl]heptanoic acid (3),

racemic 7-[ 3oz,5a-peroxy-2;8-( 3-hydroperoxy-4- methyl-1-octenyl)-cyclopent-la-ylLheptanoic acid 3 racemic 7 301,5a-peroxy-3B-methyl-2B-( 3- hydroperoxy-3-methyll octenyl )cyclopentl ayl]heptanoic acid (3),

racemic 7-[ 3a,5a-peroxyl B,2a-dimethyl-2B-( 3- hydroperoxy l -octenyl )cyclopentl a-yl ]heptanoic acid (3 and racemic 7-[3a,5a-peroxy-2B-(3-hydroperoxy-4,4-

dimethyl-l -octenyl)cyclopentl ayl]-heptanoic acid (3 is productive of the corresponding acids of formula (4), for example: racemic 8-[ 3a,5a-dihydroxy- 2/3-( 3-hydroxyl octenyl)-cyclopent-la-ylloctanoic acid (4),

racemic 6-[ 3a,5a-dihydroxy-2B-( 3 hydroxyl pentenyl )-cyclopent-l a-yHhexanoic acid (4 racemic 5-[ 3a,5a-dihydroxy-2B-( 3-hydroxyl octenyl)-cyclopc'itl a-yHpentanoic acid (4),

racemic 8-[3a,5a-dihydroxy-2B-(3-hydroxy-1- pentenyl)-cyclopentl a-ylloctanoic acid (4),

racemic 6-[3a,5a-dihydroxy-2B-(3-hydroxy-1- octeny1)-cyclopentl or-yllhexanoic acid (4),

racemic 6-[3a,5a-dihydroxy-2B-( 3-hydroxy-1- octenyl)-cyclopent-la-yl]-4-hexenoic acid (4), racemic 4-[ 3a,5a-dihydroxy-2B-( 3-hydroxy- 1 undecenyl)-cyclopentl ayl]butanoic acid (4), racemic 7-[3a,5or-dihydroxy-2/3-(3-hydroxy-loctenyl)-cyclopent-la-yl]-5-heptenoic acid (4), racemic l0-l 3a,5a-dihydroxy-2B-( 3-hydroxyl pentenyl )-cyclopentl a-yll-S-decenoic acid (4), racemic 6-[ 301,5 cr-dihydroxy-2B-( 3-hydroxyl undecenyl)-cyclopentl a-yllhexanoic acid (4), racemic 9-[ 3a,5a-dihydroxy-2B-(3-hydroxy-1- octenyl)-cyclopentla-yl 7-nonenoic acid (4), racemic 7-l3a,5a-dihydroxy-2B-(3-hydroxy-3-methyll-octenyl) cyclopent-la-yl]heptanoic acid (4), racemic 7[ 3a,5a-dihydroxy-2B-( 3-hydroxy-4-methyll-octenyl )-cyclopentl a-yll-heptanoic acid (4). racemic 7-[ 304,5 a-dihydroxy-3B-methyl-ZB-( 3- hydroxy-3methyll -octenyl )cyclopentl ayl]heptanoic acid (4).

dimethyll -octenyl )cyclopentl a-yl]-heptanoic acid EXAMPLE l0.

Racemic 7-[ 3a-hydroxy-5-oxo-2B-( 3-hydroxyl octenyl)cyclopentl a-yllheptanoic acid (racemic prosta glandin E A solution of 0. l5 g. of sodium borohydride in 3 ml. of 0.05N aqueous sodium hydroxide is added with stirring over a l5 min. period to a solution of [.0 g. of racemic 7-l 3oz,5a-peroxy-2B-( 3-hydroperoxyl octenylJcyclopent-la-yHheptanoate (3) in ml. of isopropanol at room temperature (about 25 C) under nitrogen. Stirring is continued at room temperature for about an hour. The reaction mixture is then made acid with dilute aqueous hydrochloric acid, diluted with water. and evaporated under reduced pressure until the isopropyl alcohol is removed. The aqueous residue thus obtained is extracted with ethyl acetate and the ethyl acetate extract is washed with water, then with saturated aqueous sodium chloride, dried over sodium sulfate. and evaporated under reduced pressure to give a residue comprising racemic 7-[3a,5aperoxy-2B-(3- hydroxyl -octenyl )cyclopentl a-yl ]heptanoic acid (3a).

The thus obtained residue comprising racemic 7- [301,5 a-peroxy-2[3-( 3-hydroxy- -octenyl )cyclopent- Izx-yH-heptanoic acid is dissolved in about 40 ml. of hexane and absorbed on 40 g. of slightly basic chromatographic alumina. The column is allowed to stand for about 5 hr., then is eluted with methanol and the eluate is evaporated to give a residue comprising racemic 7-[3a-hydroxy-5-oxo-2,B-(3-hydroxy-1- octenyl)cyclopent-la-yU-heptanoic acid (5). The residue is dissolved in a small amount of ethyl acetate and chromatographed over 100 g. of acid washed silica gel. The chromatogram is eluted with ethyl acetate containing increasing percentages of methanol and the eluate fractions are evaporated. The thus obtained residues are analyzed by thin layer chromatography to select the fractions comprising racemic 7-[3oz-hydroxy-5-oxo-2B- (3-hydroxy-1-octenyl) cyclopent-la-yllheptanoic acid (5). The thus obtained product can be further purified by repeated chromatography, preparative thin layer chromatography, counter-current extraction, and crystallization, or by a combination of the above methods.

Following the procedure of Example 10 but substitut ing for racemic 7-l 3a,5a-peroxy-2B-( 3-hydroperoxyl octenyljcyclopent-la-yl]heptanoic acid (3) as starting material other acids of formula 3, for example those named following Example 9, is productive of the corre sponding acids of formula 5, for example: racemic 8- [3a-hydroxy-5-oxo-2B-(3-hydroxy-l-octenyl)-cyclopent-loz-yHoctanoic acid (5), racemic 6-[3a-hydroxy-5-oxo-2B-(3-hydroxy-lpentenyl )-cyclopent-la-yl1hexanoic acid (5 racemic S-i 3a-hydroxy-S-oxo-2B-( 3-hydroxyloctenyl)-cycl0pent-Ia-yHpentanoic acid (5), racemic 8[ 3a-hydroxy-5-oxo2,8-( 3-hydroxyl pentenyU-cyclopenvla-ylloctanoic acid (5), racemic 6 3a-hydroxy-5-oxo-2B-(3-hydroxy-1- octenyl)cyclopent-la-yllhexanoic acid (5).

30 racemic 6-[ 3a-hydroxy-5-oxo-2B-( 3-hydroxyl octenyl )cyclopentl oz-yl ]-4-hexenoic acid 5 racemic 4-[ 3a-hydroxy-5-oxo-2B-( 3-hydroxyl undecenyl )-cyclopentl a-yllbutanoic acid (5 racemic 7-l 3a-hydroxy-5-oxo-2,B-( 3-hydroxyl octenyl )-c vclopent- I a-yl l-5-heptenoic acid (5 racemic lU-l 3a-hydroxy 5-oxo-2B-( 3-hydroxyl pentenyl )-cyclopentl a-yl 1-8-decenoic acid (5 racemic o-l 3a-hydroxy-5-oxo-2,B( S-hydroxy- 1 undecenyl)-cyclopent-la-yllhexanoic acid (5). racemic 9-[ 3a-hydroxy-5-oxo-2B-( 3-hydroxyl octenyl )-cyclopentl oz-yl ]-7-nonenoic acid (5 racemic 7-[ 3a-hydroxy-5-oxo-2B-( 3-hydroxy-3- methyl-1-octenyl)-cyclopentla-yl]heptanoic acid (5 racemic 7-[3a-hydroxy-5-oxo-2B-( 3-hydroxy-4- methyll -octenyl )-cyclopent- 1 a-yl l-heptanoic acid racemic 7-[ 3a-hydroxy-5-oxo-3B-methyl-2/3-( 3- hydroxy-3-methyll -octenyl )cyclopentlayllheptanoic acid (5),

racemic 7-[3a-hydroxy-5-oxo-lB,2a-dimethyl-2B-(3- hydroxy-B-methyl-1-octenyl)cyclopentlayUheptanoic acid (5),

racemic 7-[3a-hydroxy-5-oxo-lB,2a-dimethyl-2B-(3- hydroxyl -octenyl )cyclopent l a-yl ]heptanoic acid (5). and

racemic 7-[3a-hydroxy-5-oxo-2B-(3-hydroxy -4,4- dimethyll-octenyl)-cyclopentl ayl ]-heptanoic acid Example ll.

Racemic 7-[3a,5a-dihydroxy-2B-(2-octenyl)-cyclopent-la-yHheptanoic acid 8).

Following the procedure of Example 9 but substituting racemic 7-[3a,5a-peroxy-2B-(2-octenyl)-cyclopent-la-yl1heptanoic acid (2) for racemic 7-[3o:,5aperoxy-2B( 3-hydroperoxyl -octenyl )cyclopentl ayl]heptanoic acid (3) as starting material is productive of racemic 7-[3oz,5a-dihydroxy-2B-(2-octenyl)-cyclopent-la-yllheptanoic acid (8).

Following the procedure of Example 9 but substituting for racemic 7-[ 301,5 a-peroxy-2B-( 3-hydroperoxy l octenyl)cyclopent-la-yl]heptanoic acid (3) as starting material compounds of formula 2, for example: racemic8-[3a,5a-P6r0Xy-2B-( 2-octeny] )cyclopent-l ayl]octanoic acid (2), racemic 6-[3a,5a-peroxy-2B-(2-pentenyl)cyclopentla-yll-hexanoic acid (2), racemic 5-[ 3a,5a-perox y 2B-( 2-octenyl )cyclopentl ayl]-octanoic acid (2). racemic 8-[3a,50z-peroxy-2B-(Z-pentenyl)cyclopent- Ia-yH-pentanoic acid (2). racemic 6-[3a,5a-peroxy-2B-( 2-octenyl)cyclopentl ayl]-hexanoic acid (2). racemic 6-[ 301,5 a-peroxy-2B-( 2-octenyl )cyclopent- 1 0c yl] 4-hexenoic acid (2), racemic 4-[3a,5a-peroxy-2B-(2-undecenyl)cyclopentla-yll-butanoic acd (2). racemic 7-[ 3a,5a-peroxy-2B-( 2-octenyl )cyclopentl a yl]-5-heptenoic acid (2 racemic l0-{ 3a,5a-peroxy-2B-( Z-pentenyl )cyclopentla-yl1-8-decenoic acid (2), racemic 6-[3a,5a-peroxy-2,B-(Z-undecenyl)cyclopentla-yll-hexanoic acid (2), racemic 9-l 3a,5a-peroxy-2B-( 2-octenyl )cyclopentl ayl]-7-nonenoic acid 31 racemic 7-l 30:,Sa-peroxy-2B4 3-methyl-2octenyl )cyclopent-la-yl] heptanoic acid (2), racemic 7-[3a.Sa-peroxy-2B-(4-methyl-2- octenyl)cyclopent-la-yl]-heptanoic acid (2]. racemic 7-13a,5a-peroxy-3B-methyl-2B-(3-methyl-2- octenyl)cyclopent-la-yllheptanoic acid (2). racemic 7-[ 3a,5a-peroxyl B,2a-dimcthyl2,B-( 2- octenyU-cyclopentda-yl]heptanoic acid (2). and racemic 7-[3a,5a-peroxy-2B (4,4-dimethyl-2- octenyllcyclopent-lcx-yll-heptanoic acid (2), is productive of the corresponding compounds of formula 7. for example: racemic S-[3a,5a-dihydroxy-ZB-(2-octenyl)cyclopent la-yll-octanoic acid (8). racemic 6-[3a,5a-dihydroxy-2B(2- pentenyl)cyclopent-lwyH-hexanoic acid (8), racemic 5) 3a,5a-dihydroxy-2B( 2-octenyl)cyclopentla-yll-pentanoic acid (8), racemic 8-[ 3a,Sa-dihydroxy-2B-( Z-pentenyl )cyclopent la-yll-octanoic acid (8). racemic 6-[3oz,5a-dihydroxy-2B-(2-octenyl)cyclopentla-yl]-hexanoic acid (8), racemic 6-{ 3a.5or-dihydroxy-2B-( Z-octenyl )cyclopentla-yl1-4-hexenoic acid (8), racemic 4-[3a.5a-dihydroxy-2B-(2-undecenyl)cyclopent-la-yH-butanoic acid (8), racemic 7-[ 3a.Sa-dihydroxy-2B-(2-octenyl)cyclopent la-yll-S-heptenoic acid (8), racemic 10-{3a,5a-dihydroxy-2B-(2- pentenyl)cyclopent-la-yll-S-decenoic acid (8). racemic 6-[30:,5tx-dihydroxy-2B-(2- undecenyl )cyclopentl a-yl]-hexanoic acid (8). racemic 9-[3a,5a-dihydroxy-2B-(2-octenyl)cyclopentla-yll-7-nonenoic acid (8), racemic 7[ 3a,Sa-dihydroxy-2B-( 3-methyl 2- octenyl)cyclopent-la-yll-heptanoic acid (8), racemic 7 301,5 a-dihydroxy-2B-( 4-methyl-2- octenyl)cyclopent-Ia-yH-heptanoic acid (8), racemic 7-[301,5a-dihydroxy-3B-methyl-2B-(3-methyl- Z-octenyl) cyclopent-la-y]]heptanoic acid (8), racemic 7-[ 3a,5oz dihydroxyl B,20z-dimethyl-2B-( 2- octenyl)cyclopent-loz-yl]heptanoic acid (8), and racemic 7 3a,5a-dihydroxy-2B-(4,4-dimethyl-2- octenyl)cyclopent-Ia-yH-heptanoic acid (8).

EXAMPLE lZA.

Racemic 7-[3a hydroxy-5-oxo-2B-(2-octenyl)cyclopent-la-yHheptanoic acid (6).

A solution of L0 g. of racemic 7 [3a,5a-peroxy'2B' (2-octenyl)cyclopent-layl]-heptanoic acid (2) in a mixture of ml. of isopropanol and 5 ml. of pyridine is stirred under nitrogen and warmed to about 80 C. for a period of about 2 hrs. The mixture is then evaporated under reduced pressure to leave a residue which is then dissolved in ethyl acetate. and washed several times with dilute hydrochloric acid. The ethyl acetate solution is then washed with saturated aqueous sodium chloride, dried over sodium sulfate, and evaporated under reduced pressure to give a residue comprising racemic 7-[ 3a-hydroxy-5-oxo-2B4 Z-octenyl )cyclo' pent-la-yHheptanoic acid (6). The thus obtained resi due is dissolved in a small amount of ethyl acetate and chromatographed over lOO g. of acid washed silica gel. The column is eluted with ethyl acetate containing in creasing percentages of methanol. The eluate fractions are evaporated and the residues comprising racemic 7-[ 3a -hydroxy-5-oxo2B-( 2-octenyl )cyclopentl ayl]heptanoic acid are identified by TLC and infrared absorption analysis.

Following the procedure of Example 12A, but substituting for racemic 7-[3a,5a-peroxy-2B-(2-octenyl)- cyclopent-la-yll heptanoic acid (2) as starting material other acids of formula (2). for example those named following Example 1 l. is productive of the corresponding acids of formula 6, for example: racemic 8'[3a-hydroxy-5-oxo-2B-(2-octenyl)cyclopentl a-yl loctanoic acid (6), racemic 6[ 3a-hydroxy-5oxo-2B( 2pentenyl )cyclopent-la-yl] hexanoic acid (6), racemic 5-[3a-hydroxy5-oxo-2B-(2-octenyl)cyclopent-la-yllpentanoic acid (6), racemic EH3a hydroxy-5oxo-2B-(2-pentenyl)cyclopent-l a-yl]-octanoic acid (6). racemic 6[3a-hydroxy-5-oxo 2B-(2-octenyl)cyclopent-la-yHhexanoic acid (6), racemic 6-[ 3ahydroxy-5-oxo-2B-( 2-octenyl cyclopent-la-ylL4-hexenoic acid (6), racemic 4-[3a-hydroxy-5-oxo2B(2-undecenyl)cyclopentl ayl ]-butanoic acid (6), racemic 7-l3a-hydroxy-5-oxo-2B-(2- octenyl)cyclopent'la-yl]-5-heptenoic acid (6), racemic l()-{ 3a-hydroxy-5oxo-2B-( 2 pentenyl)cyclopent-l01 yl]-8-decenoic acid (6), racemic 6-( 3a-hydroxy-5-oxo-2B-( 2- undecenyl)cyclopent-la-yl]hexanoic acid (6), racemic Q-[3a-hydroxy-5-oxo 2B-(2- octenyl)cyclopent-loz-yll-7-nonenoic acid (6), racemic 7[ 3a-hydroxy-5-oxo-2B-( 3-methyl-2- octenyl)cyclopent-l a-yl]heptanoic acid (6), racemic 7-l3a-hydroxy-5-oxo-2B-(4-methyl-2- octenyl)cyclopent-la-yl]-heptanoic acid (6), racemic 7-[ 3a-hydroxy-5-oxo-3B-methyl-2B-( 3- methyl-Z-octenyl )-cyclopentl wyllheptanoic acid (6), racemic 7-l 3a-hydroxy-5-oxol B,2a-dimethyl 2B-( 2 octenyl)-cyclopent-la-yl]heptanoic acid (6), and racemic 7-[3a-hydroxy-5-oxo-2B-(4,4-dimethyl-2- octenyl)cyclopent-la-yl]-heptanoic acid (6).

EXAMPLE 12B.

Racemic 7-[3a-hydroxy-5-oxo-2B-(2-octenyl)cyclopent-la-yllheptanoic acid (6).

A solution of l g. of racemic 7-[ 3a,5oz-peroxy-2B-(2- octenyl)cyclopent-la-yl lheptanoic acid (2) in about 40 ml. of hexane is adsorbed on 40 g. of slightly basic chromatographic alumina. The column is allowed to stand for about 5 hr.. then is eluted with methanol and the eluate is evaporated to give a residue comprising racemic 7[ 3a-hydroxy-5-oxo-2B-( 2-octenyl )cyclopent-la-yllheptanoic acid (6). The thus obtained residue is dissolved in a small amount of ethyl acetate and chromatographed over g. of acid washed silica gel. The column is eluted with ethyl acetate containing increasing percentages of methanol. The eluate fractions are evaporated and the residues comprising racemic 7-[ 3rx-hydroxy5-oxo-2B-( Z-octenyl )cyclopentl ayllheptanoic acid (6) are identified by TLC and infrared absorption analysis.

Following the procedure of Example 128. but substituting for racemic 7-[ 3a,5a-peroxy-2B-( 2- octenyl lcyclopenblwyl lheptanoic acid (2) as starting material other acids of formula (2 for example those named following Example 1 l, is productive of the corresponding acids of formula 6, for example those named following Example 12A.

EXAMPLE l3.

Racemic 7-[3a.5a-dihydroxy-2B-(3-hydroxy-loctenyl) cyclopent-la-yllheptanoic acid (4) from racemic 7-[3a,Sa-dihydroxy-2B-(2-octeny)cyclopentloz-yl]-heptanoic acid (8).

A. Following the procedures of Examples l to 6, but substituting racemic 7-[ 3a,5a-dihydroxy-2B-( 2- octenyl)cyclopent-loz-yl]heptanoic acid (8) for bishomo-y-linolenic acid as starting material there is obtained racemic 7-[ 3a,5a-dihydroxy-2B-( 3- hydroperoxyl -octenyl )cyclopentl a-yl l-heptanoic acid (9).

Following the procedure of Example l3A, but substituting for racemic 7-[3a,5o:-dihydroxy-2B-(2-octenyl)- cyclopent-la-yl] heptanoic acid (8) as starting material other acids of formula 8, for example those named following Example 1 l is productive of the corresponding acids of formula 9, for example: racemic 8-(3a,5a-hydroxy-2B-(3-hydroperoxy-1- octenyl)-cyclopent-la-ylloctanoic acid (9), racemic 6-[ 301,5 a-dihydroxy-2/3-( 3-hydroperoxy- 1- pentenylrcyclopent-la-yl]hexanoic acid (9), racemic 5-[3a,5a-dihydroxy-2B-( 3-hydroperoxyl octenyl)-cyclopent-la-ylloctanoic acid (9), racemic 8-[ 301,5 a-dihydroxy-2B-( 3-hydroperoxyl pentenyU-cyclopent-loz-yllpentanoic acid (9), racemic 6-[3a,5a-dihydroxy-2B-(3-hydroperoxy-loctenyl)-cyclopent-la-yl]hexanoic acid (9), racemic 6-[ 3a,5o:-dihyd roxy-2B-( 3-hydroperoxyl octenyl)-cyclopent-la-yl]-4hexenoic acid (9), racemic 4-[3a,5a-dihydroxy-2/3-( 3-hydroperoxyl undecenyU-cyclopent-la-yl]butanoic acid (9), racemic: 7-[ 301,5 a-dihydroxy-2B-( 3-hydroperoxy- 1 octenvfi-cyclopentl a-yl]-5-heptenoic acid (9), racemic l0-[3a,5a-dihydroxy-2B-(3-hydroperoxy-lpentenyl)-cyclopent-la-yl]-8-decenoic acid (9), racemic 6-[ 3a,5a-dihydroxy-2B-( 3-hydroperoxyl undecenyhcyclopem-la-yllhexanoic acid (9), racemic 9-[3a,5a-dihydroxy-2B-(3-hydroperoxy-1- octenyl)cyclopent-la-yl]-7-nonenoic acid (9),

racemic 7-(3a,5a-dihydroxy-2B-(3-hydroperoxy-3- methyl-l-octenyl) cyclopent-la-yHheptanoic acid (9),

racemic 7-[3a,5a-dihydroxy-2B-( 3-hydroperoxy-4- methyll -octenyl)cyclopentla-yllheptanoic acid (9 racemic 7-[ 302,5 a-dihydroxy-3B-methyl-2B-( 3- hydroperoxy-3-methyll octenyl )cyclopentl ayllheptanoic acid (9), racemic 7-l 3a,5a-dihydroxyl {3,2a-dimethyl-2B-( 3- hydroperoxyl -octenyl )cyclopent- 1 a-yl ]heptanoic acid (9), and racemic 7-[3a,5a-dihydroxy-2fi-(3-hydroperoxy-4,4- dimethyll -octenyl )cyclopentl a-yl heptanoic acid (9).

B. Following the procedure of Example 9, but substituting racemic 7-l 3a,5a-dihydroxy-2B-(3-hydroperoxyl octenyl)cyclopent-la-yll heptanoic acid (9) for race mic 7-[ 301,5 a-peroxy-2B-( 3-hydroperoxyl octenylJcyclopent-la-yl1heptanoic acid (3) as starting material is productive of racemic 7-[3a,5a-dihydroxy- 2B-(B-hydroxy-l-octenyl)cyclopent-1a-yl]-heptanoic acid (4).

Following the procedure of Example l3B, but substituting for racemic 7-[ 3a,5a-dihydroxy-2/3-( 3- hydroperoxyl -octenyl )cyclopentl a-yll-heptanoic acid (9) as starting material other compounds of formula 9, for example those named following Example 13A, is productive of the corresponding acids of formula 4, for example those named following Example 9.

EXAMPLE l4.

Racemic 7-I 3a-hydroxy-5-ox0-2B-( 3-hydroxyl octenyl) cyclopent-la-yllheptanoic acid (5) from racemic 7-[3a-hydroxy-5-oxo-2/3-(2-octenyl)-cyclopentla-yl] heptanoic acid (6).

A. Following the procedures of Examples l to 6, but substituting racemic 7-[3a-hydroxy-5-oxo-2B-(2- octenyl)cyclopent-la-yl]heptanoic acid (5) for bishomo-y-linolenic acid as starting material is productive of racemic 7-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl octenyl)cyclopent-la-yl]heptanoic acid (7 Following the procedure of Example 14A, but substituting for racemic 7-{3a-hydroxy-5-oxo-2B-(2- octenyl)cyclopent-la-yl] heptanoic acid (6) as starting material other compounds of formula 6, for example those named following Example I2, is productive of the corresponding compounds of formula 7. for example: racemic 8[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxy- 1 octenyl )-cyclopent l a-yl ]octanoic acid (7 racemic 6-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl pentenyl)-cyclopent-loz-yl1hexanoic acid (7 racemic 5-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl octenyl)-cyclopentl a-yl ]pentanoic acid (7 racemic 8-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl pentenyl )-cyclopent- 1 a-yl ]octanoic acid 7), racemic 6-[3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl octenyl )-cyclopcntl a-yl]hexanoic acid (7 racemic 6-[3a-hydroxy-5-oxo-2B-(3-hydroperoxy-loctenyl)-cyclopentl a-yl l-4-hexenoic acid (7 racemie 4-[ 3a-hydr0xy-5-oxo-2B-( 3-hydroperoxyl undecenyl)-cyclopentl a-yHbutanoic acid (7), racemic 7-[3a-hydroxy-5-oxo-2/3-(3-hydroperoxyl octenyl)-cyclopent-la-yU-S-heptenoic acid (7), racemic lO-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl pentenyl)-cyclopent-la-yl]-8-decenoic acid (7), racemic 6-[3a-hydroxy-5-oxo-2B-(3-hydroperoxy-l undecenyl)-cyclopentl a-yl lhexanoic acid (7 racemic 9-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxyl octenyl)-cyclopent-la-yl]-7-nonenoic acid (7). racemic 7-[3a hydroxy-5-oxo-2B-(3-hydroperoxy-3- methyl-l-octenyl )-cyclopent-1oz-yl1heptanoic acid (7 racemic 7-[ 3a-hydroxy-5-oxo-2B-( 3-hydroperoxy-4- methyl- 1 -octenyl)-cyclopentl a-yl heptanoic acid hydroperoxy-B-methyll-octenyl )cyclopentl ayllheptanoic acid (7),

racemic 7-[3a-hydroxy-5-oxo-lB,2a-dimethyl-2B-( 3- hydroperoxyl -0ctenyl )cyclopentl a-yl ]heptanoic acid (7), and

racemic 7-[ 3a-hydroxy-5-oxo-2B-( 3- hydroperoxy-4,4- dimethyll -octenyl )cyclopentl a-yl heptanoic acid (7).

B. A solution of L0 g. of racemic 7-[3a-hydroxy-5- oxo-2B-( 3-hydroperoxyl -octenyl)cyclopent- I ayl]heptanoic acid (7) in a mixture of 20 ml. of ethanol and 5 ml. of glacial acetic acid is stirred at room temperature and 2 g. of zinc dust is added in portions over a period of about l5 minutes. The mixture is cooled to avoid a rise in temperature. After adding the zinc dust the mixture is stirred an additional 15 min., and then is filtered to remove solids. The filtrate is diluted with 40 ml. of water and the resulting mixture is concentrated until most of the ethanol is removed. The aqueous residue is then extracted with ethyl acetate and the ethyl acetate extract is washed with saturated aqueous sodium chloride, dried, and evaporated under reduced pressure to give a residue comprising racemic 7-{30zhydroxy--oxo-2B-( 3-hydroxyl-octenyl )-cyclopentla-yl] heptanoic acid (5), which can be further purified as described above, e.g., in Example 9.

Following the procedure of Example 14B, but substituting for racemic 7-[3a-hydroxy-5-oxo-2B-(3- hydroperoxyl -octeny1) cyclopentl a-yllheptanoic acid (7) as starting material other compounds of formula 7, for example those named following Example 14A, is productive of the corresponding compounds of formula 5, for example those named following Example 10.

We claim:

I. An optically active compound of the formula:

wherein W is and wherein R and R are both alkyl of one to 4 carbon atoms, inclusive.

2. An optically active compound according to claim 1 wherein 3. A compound according to claim 2 wherein R is hydrogen or alkyl of one to 4 carbon atoms, inclusive.

4. A compound according to claim 3 wherein R and R are methyl.

5. A compound according to claim 4 wherein R is hydrogen.

6. An optically active compound according to claim 1 wherein W is O=.

7. A compound according to claim 6 wherein R is hydrogen or alkyl of one to 4 carbon atoms, inclusive.

8. A compound according to claim 7 wherein R and R are methyl.

9. A compound according to claim 8 wherein R is hydrogen. 

1. AN OPTICALLY ACTIVE COMPOUND OF THE FORMULA:
 2. An optically active compound according to claim 1 wherein W is
 3. A compound according to claim 2 wherein R is hydrogen or alkyl of one to 4 carbon atoms, inclusive.
 4. A compound according to claim 3 wherein R10 and R13 are methyl.
 5. A compound according to claim 4 wherein R is hydrogen.
 6. An optically active compound according to claim 1 wherein W is O .
 7. A compound according to claim 6 wherein R is hydrogen or alkyl of one to 4 carbon atoms, inclusive.
 8. A compound according to claim 7 wherein R10 and R13 are methyl.
 9. A compound according to claim 8 wherein R is hydrogen. 